PRAVASTATIN SODIUM
- Product NDC
- 68788-7316
- 11-digit product format
- 687887316
- Labeler code
- 68788
- Product ID
- 68788-7316_268bbc5d-d6ee-4a5c-b441-acd268b76d2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2019-01-16
- 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
- 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 |
|---|
| 68788-7316-1 | 68788731601 | 100 TABLET in 1 BOTTLE (68788-7316-1) | 100 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |
| 68788-7316-2 | 68788731602 | 20 TABLET in 1 BOTTLE (68788-7316-2) | 20 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |
| 68788-7316-3 | 68788731603 | 30 TABLET in 1 BOTTLE (68788-7316-3) | 30 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |
| 68788-7316-6 | 68788731606 | 60 TABLET in 1 BOTTLE (68788-7316-6) | 60 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |
| 68788-7316-8 | 68788731608 | 120 TABLET in 1 BOTTLE (68788-7316-8) | 120 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |
| 68788-7316-9 | 68788731609 | 90 TABLET in 1 BOTTLE (68788-7316-9) | 90 tablet | 2019-01-16 | 0000-00-00 | No | No | Current |