Pravastatin Sodium
- Product NDC
- 0615-8159
- 11-digit product format
- 006158159
- Labeler code
- 0615
- Product ID
- 0615-8159_c3625468-3629-4fd9-9f3a-9a372bb5b591
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA077793
- Marketing category
- ANDA
- Marketing start
- 2018-07-12
- Marketing end
- 2022-11-30
- 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
- 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 |
|---|
| 0615-8159-39 | 00615815939 | 30 TABLET in 1 BLISTER PACK (0615-8159-39) | 30 tablet | 2018-07-12 | 2022-11-30 | No | No | Current |