simvastatin
- Product NDC
- 50090-0999
- 11-digit product format
- 500900999
- Labeler code
- 50090
- Product ID
- 50090-0999_b148490a-03bd-4d2d-9f7d-fad93c59cf61
- 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
- 20 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0999 | SIMVASTATIN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 41 | Legacy NDC | 20241127_f56da46d-30b2-4d4d-82a5-69e828088ce9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0999-1 | 50090099901 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-0999-1) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0999-2 | 50090099902 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-0999-2) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0999-3 | 50090099903 | 200 TABLET, FILM COATED in 1 BOTTLE (50090-0999-3) | 2014-11-28 | 0000-00-00 | No | No | Current |