NDC 70518-2125 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet, Coated · Oral
Product NDC70518-2125
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- May 31, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-2125-0 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0) | May 31, 2019 |
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