ZOCOR
- Product NDC
- 0006-0749
- 11-digit product format
- 000060749
- Labeler code
- 0006
- Product ID
- 0006-0749_41a60de3-6740-43c7-a8d7-7dbfd0a8d6a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SIMVASTATIN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Merck Sharp & Dohme Corp.
- Application
- NDA019766
- Marketing category
- NDA
- Marketing start
- 1991-12-23
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0006-0749-31 | 00006074931 | 30 TABLET, FILM COATED in 1 BOTTLE (0006-0749-31) | 1991-12-23 | 0000-00-00 | No | No | Current |
| 0006-0749-54 | 00006074954 | 90 TABLET, FILM COATED in 1 BOTTLE (0006-0749-54) | 1991-12-23 | 0000-00-00 | No | No | Current |