NDC 68788-9313 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC68788-9313
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- March 25, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-9313-1 | 100 TABLET, COATED in 1 BOTTLE (68788-9313-1) | Mar 25, 2015 |
| 68788-9313-3 | 30 TABLET, COATED in 1 BOTTLE (68788-9313-3) | Mar 25, 2015 |
| 68788-9313-6 | 60 TABLET, COATED in 1 BOTTLE (68788-9313-6) | Mar 25, 2015 |
| 68788-9313-9 | 90 TABLET, COATED in 1 BOTTLE (68788-9313-9) | Mar 25, 2015 |
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