NDC 29300-187 – Bisoprolol fumarate and hydrochlorothiazide
Hydrochlorothiazide 6.25 mg/1; Bisoprolol Fumarate 2.5 mg/1 · Tablet · Oral
Product NDC29300-187
Product details
- Brand name
- Bisoprolol fumarate and hydrochlorothiazide
- Generic name
- Bisoprolol fumarate and hydrochlorothiazide
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA079106
- Marketed since
- October 12, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Hydrochlorothiazide 6.25 mg/1
- Bisoprolol Fumarate 2.5 mg/1
Uses, dosage, side effects and warnings for Bisoprolol fumarate and hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 29300-187-01 | 100 TABLET in 1 BOTTLE, PLASTIC (29300-187-01) | Oct 12, 2010 |
| 29300-187-05 | 500 TABLET in 1 BOTTLE, PLASTIC (29300-187-05) | Oct 12, 2010 |
| 29300-187-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (29300-187-10) | Oct 12, 2010 |
| 29300-187-13 | 30 TABLET in 1 BOTTLE, PLASTIC (29300-187-13) | Oct 12, 2010 |
Recalls mentioning this NDC
- D-0301-2026 Feb 11, 2026 · Class II
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
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