NDC product
Pravastatin sodium
NDC 55111-229 · Dr.Reddy's Laboratories Limited
Key facts
| Product NDC | 55111-229 |
|---|---|
| Proprietary name | Pravastatin sodium |
| Nonproprietary name | Pravastatin sodium |
| Substances | PRAVASTATIN SODIUM |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Dr.Reddy's Laboratories Limited |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076714 |
| Pharmacologic classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| Marketing start | Dec 31, 2009 |
| Listing certified through | Dec 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 · Source date: