PRAVASTATIN SODIUM
- Product NDC
- 70518-0412
- 11-digit product format
- 705180412
- Labeler code
- 70518
- Product ID
- 70518-0412_a4786949-76c4-709d-e053-2995a90a1744
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2017-04-07
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0412-0 | 70518041200 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0412-0) | 90 tablet | 2017-04-07 | 0000-00-00 | No | No | Current |