pravastatin sodium
- Product NDC
- 65841-742
- 11-digit product format
- 658410742
- Labeler code
- 65841
- Product ID
- 65841-742_06a7213c-2672-47ba-86ec-58754a44504d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pravastatin sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA077751
- Marketing category
- ANDA
- Marketing start
- 2010-03-30
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 65841-742-05 | 65841074205 | 500 TABLET in 1 BOTTLE (65841-742-05) | 500 tablet | 2010-03-30 | 0000-00-00 | No | No | Current |
| 65841-742-16 | 65841074216 | 90 TABLET in 1 BOTTLE (65841-742-16) | 90 tablet | 2010-03-30 | 0000-00-00 | No | No | Current |