NDC 0093-3243 – Bisoprolol fumarate and hydrochlorothiazide
Bisoprolol Fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-3243
Product details
- Brand name
- Bisoprolol fumarate and hydrochlorothiazide
- Generic name
- Bisoprolol fumarate and hydrochlorothiazide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA020186
- Marketed since
- August 7, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Bisoprolol Fumarate 10 mg/1
- Hydrochlorothiazide 6.25 mg/1
Uses, dosage, side effects and warnings for Bisoprolol fumarate and hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-3243-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-3243-56) | Aug 7, 2019 |
Recalls mentioning this NDC
- D-0575-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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