NDC product
Norvasc
NDC 0069-1530 · PFIZER LABORATORIES DIV PFIZER INC
Key facts
| Product NDC | 0069-1530 |
|---|---|
| Proprietary name | Norvasc |
| Nonproprietary name | amlodipine besylate |
| Substances | AMLODIPINE BESYLATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | PFIZER LABORATORIES DIV PFIZER INC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA019787 |
| Pharmacologic classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
| Marketing start | Jul 31, 1992 |
| Marketing end | Jul 31, 2027 |
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