Amlodipine Besylate and Benazepril Hydrochloride
- Product NDC
- 70518-4499
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077183
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70518-4499-0 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4499-0) | 2025-10-11 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Amlodipine Besylate and Benazepril Hydrochloride | REMEDYREPACK INC. | 2025-10-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |