Pravastatin Sodium
- Product NDC
- 0615-8410
- 11-digit product format
- 006158410
- Labeler code
- 0615
- Product ID
- 0615-8410_3179a670-fe5e-47bc-b1ce-db4be693131f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA077987
- Marketing category
- ANDA
- Marketing start
- 2007-12-28
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8410-39 | 00615841039 | 30 TABLET in 1 BLISTER PACK (0615-8410-39) | 30 tablet | 2021-10-18 | 0000-00-00 | No | No | Current |