PRAVACHOL
- Product NDC
- 0003-5194
- 11-digit product format
- 000035194
- Labeler code
- 0003
- Product ID
- 0003-5194_94e23dcc-1a10-4e2f-80e3-9b1d15bd9d89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Application
- NDA019898
- Marketing category
- NDA
- Marketing start
- 2009-06-01
- Marketing end
- 2021-10-31
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0003-5194-10 | 00003519410 | 90 TABLET in 1 BOTTLE (0003-5194-10) | 90 tablet | 2009-06-01 | 2021-10-31 | No | No | Current |