Clopidogrel
- Product NDC
- 68788-7463
- 11-digit product format
- 687887463
- Labeler code
- 68788
- Product ID
- 68788-7463_132768e0-1d00-4134-8dcb-df939a4f6cd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202925
- Marketing category
- ANDA
- Marketing start
- 2013-11-21
- Marketing end
- 0000-00-00
- Substance
- CLOPIDOGREL BISULFATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 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 |
|---|
| 68788-7463-3 | 68788746303 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7463-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7463-6 | 68788746306 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7463-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7463-9 | 68788746309 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7463-9) | 2019-12-27 | 0000-00-00 | No | No | Current |