Pravastatin Sodium
- Product NDC
- 42291-668
- 11-digit product format
- 422910668
- Labeler code
- 42291
- Product ID
- 42291-668_ec190869-82b8-6c7f-e053-2a95a90a8577
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pravastatin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA076056
- Marketing category
- ANDA
- Marketing start
- 2014-06-30
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-668 | PRAVASTATIN SODIUM TABLET [AVKARE] | 12 | Legacy NDC | 20230913_345979e5-647b-7898-a933-e43a25250627.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-668-10 | 42291066810 | 1000 TABLET in 1 BOTTLE (42291-668-10) | 1000 tablet | 2014-06-30 | 0000-00-00 | No | No | Current |
| 42291-668-90 | 42291066890 | 90 TABLET in 1 BOTTLE (42291-668-90) | 90 tablet | 2014-06-30 | 0000-00-00 | No | No | Current |