NDC 30698-449 – Lotensin
Benazepril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC30698-449
Product details
- Brand name
- Lotensin
- Generic name
- Benazepril hydrochloride
- Labeler
- Validus Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA · NDA019851
- Marketed since
- June 21, 1991
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 20 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 30698-449-01 | 100 TABLET in 1 BOTTLE (30698-449-01) | Jun 21, 1991 |