NDC product
Amlodipine Besylate and Benazepril Hydrochloride
NDC 50090-5389 · A-S Medication Solutions
Key facts
| Product NDC | 50090-5389 |
|---|---|
| Proprietary name | Amlodipine Besylate and Benazepril Hydrochloride |
| Nonproprietary name | Amlodipine Besylate and Benazepril Hydrochloride |
| Substances | AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | A-S Medication Solutions |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA078466 |
| Pharmacologic classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE] and 2 more |
| Marketing start | Oct 4, 2018 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: