PRAVASTATIN SODIUM
- Product NDC
- 68071-3247
- 11-digit product format
- 680713247
- Labeler code
- 68071
- Product ID
- 68071-3247_bb14cafb-a901-5b6a-e053-2995a90ab47a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2017-02-16
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 20 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 |
|---|
| 68071-3247-3 | 68071324703 | 30 TABLET in 1 BOTTLE (68071-3247-3) | 30 tablet | 2017-05-09 | 0000-00-00 | No | No | Current |
| 68071-3247-9 | 68071324709 | 90 TABLET in 1 BOTTLE (68071-3247-9) | 90 tablet | 2017-05-09 | 0000-00-00 | No | No | Current |