PRAVASTATIN SODIUM
- Product NDC
- 70518-1902
- 11-digit product format
- 705181902
- Labeler code
- 70518
- Product ID
- 70518-1902_c50c688f-6638-1ffa-e053-2a95a90a2114
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- 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
- 2022-12-31
- 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 |
|---|
| 70518-1902-0 | 70518190200 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1902-0) | 90 tablet | 2019-02-22 | 0000-00-00 | No | No | Current |
| 70518-1902-1 | 70518190201 | 30 TABLET in 1 BLISTER PACK (70518-1902-1) | 30 tablet | 2019-03-13 | 0000-00-00 | No | No | Current |