simvastatin
- Product NDC
- 50090-1000
- 11-digit product format
- 500901000
- Labeler code
- 50090
- Product ID
- 50090-1000_232b024c-a231-4497-9d8c-9ffa5b19e6c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- simvastatin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078155
- Marketing category
- ANDA
- Marketing start
- 2008-02-26
- Marketing end
- 0000-00-00
- Substance
- SIMVASTATIN
- Active strength
- 40 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1000-0 | 50090100000 | 1000 TABLET, FILM COATED in 1 BOTTLE (50090-1000-0) | 2018-11-02 | 0000-00-00 | No | No | Current |
| 50090-1000-1 | 50090100001 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1000-1) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1000-2 | 50090100002 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-1000-2) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1000-3 | 50090100003 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1000-3) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1000-4 | 50090100004 | 200 TABLET, FILM COATED in 1 BOTTLE (50090-1000-4) | 2014-11-28 | 0000-00-00 | No | No | Current |