Clopidogrel
- Product NDC
- 64980-343
- 11-digit product format
- 649800343
- Labeler code
- 64980
- Product ID
- 64980-343_cedc26ea-ef6c-4136-a921-2d702f9484b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 64980-343-03 | 64980034303 | 30 TABLET, FILM COATED in 1 BOTTLE (64980-343-03) | 2012-05-17 | 0000-00-00 | No | No | Current |
| 64980-343-09 | 64980034309 | 90 TABLET, FILM COATED in 1 BOTTLE (64980-343-09) | 2012-05-17 | 0000-00-00 | No | No | Current |
| 64980-343-50 | 64980034350 | 500 TABLET, FILM COATED in 1 BOTTLE (64980-343-50) | 2012-05-17 | 0000-00-00 | No | No | Current |