Pravastatin Sodium
- Product NDC
- 70518-2986
- 11-digit product format
- 705182986
- Labeler code
- 70518
- Product ID
- 70518-2986_d3d36d4a-6b6f-f1e0-e053-2995a90ac27c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077793
- Marketing category
- ANDA
- Marketing start
- 2021-01-08
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 80 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2986-0 | 70518298600 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2986-0) | 90 tablet | 2021-01-08 | 0000-00-00 | No | No | Current |