Amlodipine and Benazepril Hydrochloride
- Product NDC
- 23155-921
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA091431
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 23155-921-01 | 100 CAPSULE in 1 BOTTLE (23155-921-01) | 2026-05-23 | | No | Historical |
| 23155-921-05 | 500 CAPSULE in 1 BOTTLE (23155-921-05) | 2026-05-23 | | No | Historical |
| 23155-921-10 | 1000 CAPSULE in 1 BOTTLE (23155-921-10) | 2026-05-23 | | No | Historical |