Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg Technical Specification:
Product Name: | Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP |
Brand Name: | Generic |
Strength: | (2.5mg+6.25mg), (5mg+6.25mg), (5mg+12.5mg), (10mg+6.25mg) |
Dosage Form: | Tablets (film-coated) |
Route of Administration: | Via Oral Route |
Packing: | 10s, 30s, 100s, 500s |
Pack Insert/Leaflet: | PIL (Patient Information Leaflet), SmPC (Summary Product Characteristics) |
Regulatory Documents: | COA, MOA, COPP, FSC, Stability Studies, GMP, CTD Dossier |
Therapeutic use: | Antihypertensive |
Indication: | Bisoprolol Fumarate and Hydrochlorothiazide is indicated for the treatment of hypertension. It combines two antihypertensive agents in a once-daily dosage: a synthetic beta1 selective (cardioselective) adrenoceptor blocking agent (bisoprolol fumarate) and a benzothiadiazine diuretic (hydrochlorothiazide). |
Storage: | Store at 20°C to 25°C (68°F to 77°F). Store in dry place protected from light and moisture. |
GENERIC NAME OF THE MEDICINAL PRODUCT:
- Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
QUALITATIVE AND QUANTITATIVE COMPOSITION:
- Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….10mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Sunset yellow lake
THERAPEUTIC INDICATIONS:
Bisoprolol Fumarate and Hydrochlorothiazide is indicated for the treatment of hypertension. It combines two antihypertensive agents in a once-daily dosage: a synthetic beta1 selective (cardioselective) adrenoceptor blocking agent (bisoprolol fumarate) and a benzothiadiazine diuretic (hydrochlorothiazide).
CAUTION & WARNING:
CAUTION: Read enclosed leaflet before use.
Keep medicine out of reach of children.
SWALLOW WHOLE DO NOT CHEW OR CRUSH.
DISPENSE IN A TIGHT CONTAINER.
TAKE THIS PREPARATION IN THE MORNING WITH OR WITHOUT FOOD.
IT IS DANGEROUS TO TAKE THIS PREPARATION EXCEPT UNDER MEDICAL SUPERVISION.
Warning: To be sold by retail on the prescription of a Registered Medical Practitioner only.
STORAGE & DOSAGE:
Storage: Store at 20°C to 25°C (68°F to 77°F)
Store in dry place protected from light and moisture.
Dosage: As directed by the Physician
Attach dispensing label as per end country.
GENERIC NAME OF THE MEDICINAL PRODUCT:
1. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 2.5mg+6.25mg
2. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+6.25mg
3. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+12.5mg
4. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
2. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+6.25mg
3. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+12.5mg
4. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
QUALITATIVE AND QUANTITATIVE COMPOSITION:
1. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 2.5mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….2.5mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Ferric oxide red
2. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….5mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Ferric oxide yellow
3. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+12.5mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….5mg
Hydrochlorothiazide USP………………….12.5mg
Excipients……………………..………………… q.s
Colour: Sunset yellow
4. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….10mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Sunset yellow lake
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….2.5mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Ferric oxide red
2. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….5mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Ferric oxide yellow
3. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 5mg+12.5mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….5mg
Hydrochlorothiazide USP………………….12.5mg
Excipients……………………..………………… q.s
Colour: Sunset yellow
4. Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 10mg+6.25mg
Each film-coated tablet contains:
Bisoprolol Fumarate USP………………….10mg
Hydrochlorothiazide USP………………….6.25mg
Excipients……………………..………………… q.s
Colour: Sunset yellow lake
THERAPEUTIC INDICATIONS:
Bisoprolol Fumarate and Hydrochlorothiazide is indicated for the treatment of hypertension. It combines two antihypertensive agents in a once-daily dosage: a synthetic beta1 selective (cardioselective) adrenoceptor blocking agent (bisoprolol fumarate) and a benzothiadiazine diuretic (hydrochlorothiazide).
CAUTION & WARNING:
CAUTION: Read enclosed leaflet before use.
KEEP MEDICINE OUT OF REACH OF CHILDREN.
SWALLOW WHOLE DO NOT CHEW OR CRUSH.
DISPENSE IN A TIGHT CONTAINER.
TAKE THIS PREPARATION IN THE MORNING WITH OR WITHOUT FOOD.
IT IS DANGEROUS TO TAKE THIS PREPARATION EXCEPT UNDER MEDICAL SUPERVISION.
WARNING: To be sold by retail on the prescription of a Registered Medical Practitioner only.
KEEP MEDICINE OUT OF REACH OF CHILDREN.
SWALLOW WHOLE DO NOT CHEW OR CRUSH.
DISPENSE IN A TIGHT CONTAINER.
TAKE THIS PREPARATION IN THE MORNING WITH OR WITHOUT FOOD.
IT IS DANGEROUS TO TAKE THIS PREPARATION EXCEPT UNDER MEDICAL SUPERVISION.
WARNING: To be sold by retail on the prescription of a Registered Medical Practitioner only.
STORAGE & DOSAGE:
Storage: Store at 20°C to 25°C (68°F to 77°F)
Store in dry place protected from light and moisture.
Dosage: As directed by the Physician
Attach dispensing label as per end country.
Store in dry place protected from light and moisture.
Dosage: As directed by the Physician
Attach dispensing label as per end country.