NDC product
SPIRONOLACTONE
NDC 63629-1065 · Bryant Ranch Prepack
Key facts
| Product NDC | 63629-1065 |
|---|---|
| Proprietary name | SPIRONOLACTONE |
| Nonproprietary name | SPIRONOLACTONE |
| Substances | SPIRONOLACTONE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Bryant Ranch Prepack |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA089424 |
| Pharmacologic classes | Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA] |
| Marketing start | Jul 23, 1986 |
| Marketing end | Feb 28, 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