NDC 71335-0595 – Bisoprolol fumarate and hydrochlorothiazide
Hydrochlorothiazide 6.25 mg/1; Bisoprolol Fumarate 5 mg/1 · Tablet · Oral
Product NDC71335-0595
Product details
- Brand name
- Bisoprolol fumarate and hydrochlorothiazide
- Generic name
- Bisoprolol fumarate and hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA079106
- Marketed since
- October 12, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Hydrochlorothiazide 6.25 mg/1
- Bisoprolol Fumarate 5 mg/1
Uses, dosage, side effects and warnings for Bisoprolol fumarate and hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0595-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-0595-1) | Jun 25, 2018 |
| 71335-0595-2 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-0595-2) | Mar 19, 2019 |
| 71335-0595-3 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-0595-3) | May 23, 2024 |
| 71335-0595-4 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-0595-4) | Jul 19, 2023 |
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