PRAVASTATIN SODIUM
- Product NDC
- 70518-1157
- 11-digit product format
- 705181157
- Labeler code
- 70518
- Product ID
- 70518-1157_ebc84e3e-6730-34c2-e053-2995a90a073d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207068
- Marketing category
- ANDA
- Marketing start
- 2018-05-02
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 10 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 |
|---|
| 70518-1157-0 | 70518115700 | 30 TABLET in 1 BLISTER PACK (70518-1157-0) | 30 tablet | 2018-05-02 | 0000-00-00 | No | No | Current |
| 70518-1157-1 | 70518115701 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1157-1) | 90 tablet | 2021-07-22 | 0000-00-00 | No | No | Current |