Composition

Each metered dose contains:
9 mcg Tiotropium Bromide (Monohydrate).

Indications

TIOTROPIUM Inhaler is indicated in the maintenance treatment of COPD.

Composition

Each actuation contains:

100/200/400 mcg Budesonide

6 mcg Formoterol (ex-valve).

Indications

FORMOTEROL/BUDESONIDE Inhaler is indicated in the regular treatment of asthma, where the use of a combination (long-acting, beta2-agonist and inhaled corticosteroid) has been found to be appropriate for instance:

Patients not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled short-acting beta2 adrenoceptor agonists.

Or:

Patients already adequately controlled on both inhaled corticosteroids and long-acting beta2 adrenoceptor agonists.

FORMOTEROL/BUDESONIDE Inhaler is also indicated as maintenance treatment of airflow obstruction in patients with COPD including chronic bronchitis and emphysema.

Composition

Each actuation delivers:

125/250 mcg of Fluticasone Propionate

Indications

Fluticasone propionate given by inhalation offers prophylactic treatment for asthma.

Adults:

Mild asthma: Patients requiring intermittent symptomatic bronchodilator asthma medication on a regular daily basis.

Moderate asthma: Patients with unstable or worsening asthma despite prophylactic therapy or bronchodilator alone.

Severe asthma: Patients with severe chronic asthma and those who are dependent on systemic corticosteroids for adequate control of symptoms. On introduction of inhaled fluticasone propionate many of these patients may be able to reduce significantly, or to eliminate, their requirement for oral corticosteroids.

Children:

Any child who requires prophylactic medication, including patients not controlled on currently available prophylactic medication.

Composition

Each dose  contains:

120 mcg salbutamol sulphate

(equivalent to 100 mcg salbutamol),

50 mcg beclomethasone dipropionate.

Indications

Treatment of obstructive airway disease, especially intended for patients who require regular doses of both drugs.

Composition

Each actuation meters:

21 mcg of ipratropium bromide 120 mcg of salbutamol sulfate from the valve and delivers 18 mcg of ipratropium bromide and 103 mcg of salbutamol sulfate (equivalent to 90 mcg salbutamol base) from the mouthpiece.

Indications

IPRATAMOL is indicated for use in patients with chronic obstructive pulmonary disease (COPD) on a regular aerosol bronchodilator who continue to have evidence of bronchospasm and who require a second bronchodilator.

Composition

Each actuation of the inhaler delivers:

67.8 mcg of levosalbutamol tartrate (equivalent to 51.6 mcg of levosalbutamol free base) from the valve and 59 mcg of levosalbutamol tartrate (equivalent to 45 mcg of levosalbutamol free base) from the actuator mouthpiece.

Indications

Bronchospasm:

LEVOSAL is indicated for the treatment or prevention of bronchospasm in adults, adolescents, and children 4 years of age and older with reversible obstructive airway disease.

Composition

Each actuation delivers :

25 mcg of salmeterol base (as salmeterol xinafoate) from the valve 

21 mcg of salmeterol base (as salmeterol xinafoate) from the actuator.

Indications

Asthma:

Salmeterol Inhalation Aerosol is indicated for long-term, twice-daily (morning and evening) administration in the maintenance treatment of asthma and in the prevention of bronchospasm in patients 12 years of age and older with reversible obstructive airway disease, including patients with symptoms of nocturnal asthma, who require regular treatment with inhaled, short-acting beta2-agonists. It should not be used in patients whose asthma can be managed by occasional use of inhaled, short-acting beta2-agonists.

Salmeterol Inhalation Aerosol may be used alone or in combination with inhaled or systemic corticosteroid therapy.

Salmeterol Inhalation Aerosol is also indicated for prevention of exercise-induced bronchospasm in patients 12 years of age and older.

Chronic Obstructive Pulmonary Disease:

Salmeterol Inhalation Aerosol is indicated for long-term, twice daily (morning and evening) administration in the maintenance treatment of bronchospasm associated with COPD (including emphysema and chronic bronchitis).

Composition

Each metered dose (ex-valve) contains:

100 micrograms of Beclomethasone dipropionate and 6 micrograms of formoterol fumarate dihydrate.

Excipients: HFA 134a, anhydrous ethanol, Hcl. 

Indications

Beclolide plus is indicated in the regular treatment of asthma where use of a combination product (inhaled corticosteroid and long-acting beta2-agonist) is appropriate:

- patients not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled rapid-acting beta2-agonist or

- patients already adequately controlled on both inhaled corticosteroids and long-acting beta2- agonists.

This product is indicated in adults.

Composition

each actuation delivers 80 / 160 mcg ciclesonide from the mouthpiece.

Indications

Treatment to control persistent asthma in adults and adolescents (12 years and older).

Composition

Each actuation contains: 9 mcg Tiotropium (as tiotropium bromide monohydrate) + 6mcg Formoterol fumarate dihydrate.

Excipients: HFA134a

Indications

Tio plus is indicated in the maintenance treatment of COPD (chronic obstructive pulmonary disease).

Composition

each prolonged release capsule contain:

phenylephrine  20 mg + loratadine 5 mg

as prolonged release pellets.

Indications

Common cold, hay fever (allergic rhinitis) or other upper respiratory allergies

Composition

Each capsule contains :

5 mg Phenylephrine HCl

2.5 mg Triprolidine HCl

Excipients: magnesium stearate, Microcrystalline cellulose, sodium starch glycolate. 

Indications

Temporarily relieves these symptoms due to common cold, hay fever (allergic rhinitis) or other upper Respiratory allergies:

• Runny nose.

• Sneezing.

• Itching of the nose or throat.

• Itchy, watery eyes.

• Nasal congestion.

• Reduces swelling of nasal passages.

Composition

Each prolonged release capsule contains 8,16,24mg galantamine (as hydrobromide ) 

 excipients: as pellets 

Indications

Galantamine is indicated for the symptomatic treatment of mild to moderately severe dementia of the Alzheimer.

Composition

Each delayed release capsule contains enteric coated pellets of:

22.4mg duloxetine hydrochloride eq: 20 mg duloxetine.

33.7 mg duloxetine hydrochloride eq: 30 mg duloxetine.

67.3 mg duloxetine hydrochloride eq: 60 mg duloxetine. 

Indications

- DULOXETINE is indicated for the treatment of major depressive disorder (MDD).

- DULOXETINE is indicated for the acute treatment of generalized anxiety disorder (GAD).

- DULOXETINE is indicated for the management of neuropathic pain associated with diabetic peripheral neuropathy (DPNP).

- DULOXETINE is indicated for the management of fibromyalgia (FM).

- DULOXETINE is indicated for the management of the Chronic Musculoskeletal Pain.

Composition

Each capsule contains: 10mg or 20mg Fluoxetine 

Excipients: anhydrous colloidal silica, Maize starch, Talc, magnesium stearate. 

Indications

Adults:

1- Major depressive episodes.

2- Obsessive-compulsive disorder.

3-Bulimia nervosa: Fluoxetine is indicated as a complement of psychotherapy for the reduction of binge-eating and purging activity. 

Children and Adolescents Aged 8 Years and Above:

Moderate to severe major depressive episode, if depression is unresponsive to psychological therapy after 4-6 sessions, antidepressant medication should be offered to a child or young person with moderate to severe depression only in combination with a concurrent psychological therapy.

Composition

Zinc oxide11.3g , mineral oil, beeswax, microcrystalline wax, synthetic beeswax, fragrance, sorbitan sesquioleate, oenothera biennis (evening primrose) seed extract, olea europaea (olive) leaf extract, dimethicone, tocopherol, methylparaben, glycine soja (soybean) oil, propylparaben, panthenol, sarcosine, benzoic acid, potassium aspartate, potassium hydroxide, magnesium aspartate, sodium cocoyl amino acids, water.

Indications

Z-Aqua cream helps: 

• helps relieve and prevent rashes and irritation due to wetness from incontinence.

• helps to relief chafed skin resulting from  irritation and helps seal out moisture of the skin. 

Composition

texapon, cremophor RH40, perfume, water

Indications

Cidal preparations are used for the cases of infestation

with Sarcoptes scabies (scabies)and lice.

Composition

Each gram of the Cream contains 1.2 mg betamethasone valerate (equivalent to 1 mg Betamethasone)

Indications

Betamethasone Allied is a potent topical corticosteroid indicated for adults, elderly and children over 1 year for the relief of the inflammatory and pruritic manifestations of steroid responsive dermatoses. These include the following:

• Atopic dermatitis (including infantile atopic dermatitis). 

• Nummular dermatitis (discoid eczema).

• Prurigo nodularis .

• Psoriasis (excluding widespread plaque psoriasis).

• Lichen simplex chronicus (neurodermatitis) and lichen planus. 

• Seborrhoeic dermatitis.

• Irritant or allergic contact dermatitis. 

• Discoid lupus erythematosus .

• Adjunct to systemic steroid therapy in generalized erythroderma.

• Insect bite reactions.

Composition

Each capsule contains Chlorpheniramine Maleate 4mg, Ibuprofen 200mg, 

Phenylephrine Hydrochloride 10mg.

Indications

• Temporarily relieves these symptoms associated with hay fever or other upper respiratory allergies, and the common cold:

• Runny nose, itchy, watery eyes, itching of the nose or throat.

• Sneezing, nasal congestion, sinus pressure.

• Headache, fever, minor body aches and pains.

• Reduces swelling of the nasal passages.

• Temporarily restores freer breathing through the nose.

Composition

One capsule (pellets) contains: 125mg Aprepitant. 

Two capsules (pellets) contains: 80 mg Aprepitant.

Indications

1. Prevention of Chemotherapy Induced Nausea and Vomiting (CINV): the capsules, in combination with other antiemetic agents, are indicated in patients 12 years of age and older for the prevention of: 

• Acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin. 

• Nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC).

2. Prevention of Postoperative Nausea and Vomiting (PONV) in adults

Composition

Each spray contains budesonide 64 micrograms (1.28 mg/ml).

Excipients: Dispersible cellulose (Microcrystalline cellulose and carboxymethylcellulose sodium, Polysorbate 80 , Potassium sorbate, dextrose, anhydrous, Disodium edetate, Hydrochloric acid, Ascorbic acid, Purified water.

Indications

Seasonal and perennial allergic rhinitis and vasomotor rhinitis. Treatment of nasal polyps.

Composition

Each 1 g of cream contains:

10 mg clotrimazole.

Indications

clotrimazole Cream is used to treat fungal skin infections such as ringworm, athlete’s foot, fungal nappy rash and fungal sweat rash. It is also used to relieve irritation of the vulva (external thrush) or the end of the penis, which may be associated with thrush.

Composition

Each 1g Gel Contains 75 mg Dapsone.

Excipients: Diethylene Glycol Monoethyl Ether, Methylparaben, Polysorbate 80, Acrylamide, Isohexadecane, Purified Water.

Indications

It is used for topical treatment of acne vulgaris.

Composition

Each metered dose contains 50 micrograms of fluticasone propionate.

Excipients: 0.02% w/w benzalkonium chloride, dextrose, microcrystalline cellulose and carboxymethylcellulose sodium, 0.25% w/w phenylethyl alcohol and polysorbate 80.

Indications

The prophylaxis and treatment of seasonal allergic rhinitis (including hay fever) and perennial rhinitis. Fluticasone propionate has potent anti-inflammatory activity but when used topically on the nasal mucosa has no detectable systemic activity.

Composition

Minoxidil 5%, sodium laurel sulfate, Diethanolamine DEA, Coconut Oil, Glycerin, hydroxyethyl cellulose, Propylene Glycol, Provitamin B5, Vitamin B6, EDTA, Palmitate Vitamin A, Deionized water

Indications

A shampoo that helps increase hair growth, in addition to containing vitamin B6, it helps maintain healthy skin and scalp, thus promoting better hair growth.

Composition

The  0.1% xylometazoline hydrochloride Nasal Spray, nasal solution contains 1 mg/ml of xylometazoline hydrochloride. Each metered-dose spray delivers 0.14 mg of xylometazoline hydrochloride.

excipients: sodium chloride, Disodium phosphate dodecahydrate (Sodium phosphate ) , Sodium dihydrogen phosphate dihydrate (Sodium acid phosphate), disodium edetate, benzalkonium chloride and water .

Indications

For the symptomatic relief of nasal congestion, perennial and allergic rhinitis (including hay fever), sinusitis.