PRAVASTATIN SODIUM
- Product NDC
- 60760-421
- 11-digit product format
- 607600421
- Labeler code
- 60760
- Product ID
- 60760-421_f06e92a0-b49e-0364-e053-2a95a90a7b3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2018-03-13
- 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 |
|---|
| 60760-421-90 | 60760042190 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-421-90) | 90 tablet | 2018-03-13 | 0000-00-00 | No | No | Current |