NDC 71335-1769 – Bisoprolol Fumarate and Hydrochlorothiazide
Bisoprolol Fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1769
Product details
- Brand name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212678
- Marketed since
- April 30, 2019
- Listing expires
- December 31, 2027
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1769-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1769-1) | Feb 2, 2021 |
| 71335-1769-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1769-2) | Dec 29, 2021 |
| 71335-1769-3 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1769-3) | Dec 29, 2021 |
| 71335-1769-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1769-4) | Apr 5, 2024 |
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