NDC product
Pravastatin Sodium
NDC 35356-919 · Lake Erie Medical DBA Quality Care Products LLC
Key facts
| Product NDC | 35356-919 |
|---|---|
| Proprietary name | Pravastatin Sodium |
| Nonproprietary name | pravastatin sodium |
| Substances | PRAVASTATIN SODIUM |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Lake Erie Medical DBA Quality Care Products LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076341 |
| Pharmacologic classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| Marketing start | Jul 18, 2011 |
| Marketing end | Apr 30, 2028 |
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