NDC 68462-878 – Bisoprolol Fumarate and Hydrochlorothiazide
Bisoprolol Fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-878
Product details
- Brand name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Labeler
- GLENMARK PHARMACEUTICALS INC., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215995
- Marketed since
- January 26, 2022
- 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 |
|---|---|---|
| 68462-878-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68462-878-01) | Jan 26, 2022 |
| 68462-878-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68462-878-05) | Jan 26, 2022 |
| 68462-878-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-878-30) | Jan 26, 2022 |
Recalls mentioning this NDC
- D-0199-2026 Dec 10, 2025 · Class III
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe - D-0085-2024 Nov 8, 2023 · Class III
Failed Impurities/Degradation Specifications
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