NDC 70771-1761 – Bisoprolol Fumarate and Hydrochlorothiazide
Bisoprolol Fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral
Product NDC70771-1761
Product details
- Brand name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- Bisoprolol fumarate and hydrochlorothiazide
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215666
- Marketed since
- March 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Bisoprolol Fumarate 5 mg/1
- Hydrochlorothiazide 6.25 mg/1
Uses, dosage, side effects and warnings for Bisoprolol fumarate and hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1761-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1761-1) | Mar 1, 2023 |
| 70771-1761-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1761-3) | Mar 1, 2023 |
| 70771-1761-5 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1761-5) | Mar 1, 2023 |
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