NDC 70954-413 – Bisoprolol Fumarate and Hydrochlorothiazide
Bisoprolol Fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet · Oral
Product NDC70954-413
Product details
- Brand name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- Bisoprolol Fumarate and Hydrochlorothiazide
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA215562
- Marketed since
- November 4, 2021
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70954-413-10 | 30 TABLET in 1 BOTTLE (70954-413-10) | Nov 4, 2021 |
| 70954-413-30 | 100 TABLET in 1 BOTTLE (70954-413-30) | Nov 4, 2021 |
| 70954-413-40 | 500 TABLET in 1 BOTTLE (70954-413-40) | Nov 4, 2021 |
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