pravastatin sodium
- Product NDC
- 65841-740
- 11-digit product format
- 658410740
- Labeler code
- 65841
- Product ID
- 65841-740_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
- 20 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65841-740-05 | 65841074005 | 500 TABLET in 1 BOTTLE (65841-740-05) | 500 tablet | 2010-03-30 | 0000-00-00 | No | No | Current |
| 65841-740-10 | 65841074010 | 1000 TABLET in 1 BOTTLE (65841-740-10) | 1000 tablet | 2010-03-30 | 0000-00-00 | No | No | Current |
| 65841-740-16 | 65841074016 | 90 TABLET in 1 BOTTLE (65841-740-16) | 90 tablet | 2010-03-30 | 0000-00-00 | No | No | Current |