Clopidogrel
- Product NDC
- 61919-737
- 11-digit product format
- 619190737
- Labeler code
- 61919
- Product ID
- 61919-737_8026fded-44ee-36ce-e053-2991aa0aa770
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090494
- Marketing category
- ANDA
- Marketing start
- 2019-01-23
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-737-90 | 61919073790 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-737-90) | 2019-01-23 | 0000-00-00 | No | No | Current |