Clopidogrel
- Product NDC
- 68788-8190
- 11-digit product format
- 687888190
- Labeler code
- 68788
- Product ID
- 68788-8190_272228a1-84b6-4263-9bb5-3385f8778ccd
- 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
- 2022-05-16
- Marketing end
- 0000-00-00
- Substance
- CLOPIDOGREL BISULFATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-8190-3 | 68788819003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8190-3) | 2022-05-16 | 0000-00-00 | No | No | Current |
| 68788-8190-6 | 68788819006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8190-6) | 2022-05-16 | 0000-00-00 | No | No | Current |
| 68788-8190-9 | 68788819009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8190-9) | 2022-05-16 | 0000-00-00 | No | No | Current |