Simvastatin
- Product NDC
- 71335-2147
- 11-digit product format
- 713352147
- Labeler code
- 71335
- Product ID
- 71335-2147_da0e2f0f-e50c-4cd9-912c-f85d12e65dfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078034
- Marketing category
- ANDA
- Marketing start
- 2015-12-17
- Marketing end
- 0000-00-00
- Substance
- SIMVASTATIN
- Active strength
- 5 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2147-1 | 71335214701 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2147-1) | 2022-08-09 | 0000-00-00 | No | No | Current |
| 71335-2147-2 | 71335214702 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2147-2) | 2022-08-09 | 0000-00-00 | No | No | Current |
| 71335-2147-3 | 71335214703 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2147-3) | 2022-08-09 | 0000-00-00 | No | No | Current |
| 71335-2147-4 | 71335214704 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2147-4) | 2022-08-09 | 0000-00-00 | No | No | Current |