simvastatin
- Product NDC
- 68071-4996
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078155
- Marketing category
- ANDA
- Substance
- SIMVASTATIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-4996-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4996-3) | 2019-07-29 | | No | Historical |
| 68071-4996-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4996-9) | 2019-07-29 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| simvastatin | NuCare Pharmaceuticals,Inc. | 2024-06-18 | HUMAN PRESCRIPTION DRUG LABEL | 4 |