Simvastatin
- Product NDC
- 71335-1020
- 11-digit product format
- 713351020
- Labeler code
- 71335
- Product ID
- 71335-1020_778bf972-a64c-4a8b-8ac9-2cb118de681b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076052
- Marketing category
- ANDA
- Marketing start
- 2006-06-27
- Marketing end
- 0000-00-00
- Substance
- SIMVASTATIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71335-1020-1 | 71335102001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1020-1) | 2006-06-27 | 0000-00-00 | No | No | Current |
| 71335-1020-2 | 71335102002 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1020-2) | 2006-06-27 | 0000-00-00 | No | No | Current |
| 71335-1020-3 | 71335102003 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1020-3) | 2006-06-27 | 0000-00-00 | No | No | Current |
| 71335-1020-4 | 71335102004 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1020-4) | 2006-06-27 | 0000-00-00 | No | No | Current |
| 71335-1020-5 | 71335102005 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1020-5) | 2006-06-27 | 0000-00-00 | No | No | Current |
| 71335-1020-6 | 71335102006 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1020-6) | 2006-06-27 | 0000-00-00 | No | No | Current |