Clopidogrel
- Product NDC
- 57237-189
- 11-digit product format
- 572370189
- Labeler code
- 57237
- Product ID
- 57237-189_954a65d1-79ed-4705-be2d-4d7e6f13f538
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA090540
- Marketing category
- ANDA
- Marketing start
- 2012-05-17
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record