NDC 59651-678 – Bisoprolol Fumarate and Hydrochlorothiazide
Bisoprolol Fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-678
Product details
- Brand name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217922
- Marketed since
- January 21, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Bisoprolol Fumarate 2.5 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 |
|---|---|---|
| 59651-678-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-678-01) | Jan 21, 2026 |
| 59651-678-05 | 500 TABLET, FILM COATED in 1 BOTTLE (59651-678-05) | Jan 21, 2026 |
| 59651-678-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-678-30) | Jan 21, 2026 |
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