Simvastatin
- Product NDC
- 50090-6922
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077691
- Marketing category
- ANDA
- Substance
- SIMVASTATIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6922-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6922-0) | 2023-12-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Simvastatin | A-S Medication Solutions | 2023-12-25 | Human Prescription Drug Label | 1 |