Clopidogrel
- Product NDC
- 63629-6857
- 11-digit product format
- 636296857
- Labeler code
- 63629
- Product ID
- 63629-6857_c5a988b9-b074-473c-91da-f4e68315f872
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 08I79HTP27 | CLOPIDOGREL BISULFATE | 120202-66-6 | CLOPIDOGREL BISULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6857-1 | 63629685701 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6857-1) | 2015-11-25 | 0000-00-00 | No | No | Current |