Clopidogrel
- Product NDC
- 70518-1383
- 11-digit product format
- 705181383
- Labeler code
- 70518
- Product ID
- 70518-1383_92a39984-9108-b72b-e053-2a95a90a4ddb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076274
- Marketing category
- ANDA
- Marketing start
- 2018-08-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record