Amlodipine Besylate and Benazepril Hydrochloride
- Product NDC
- 50090-5404
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078466
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-5404-0 | 30 CAPSULE in 1 BOTTLE (50090-5404-0) | 2020-12-09 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Amlodipine Besylate and Benazepril Hydrochloride | A-S Medication Solutions | 2025-10-29 | HUMAN PRESCRIPTION DRUG LABEL | 7 |