Clopidogrel Bisulfate
- Product NDC
- 68788-7238
- 11-digit product format
- 687887238
- Labeler code
- 68788
- Product ID
- 68788-7238_20dd37d1-24ec-42d6-891e-bce87c7e3ab3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090494
- Marketing category
- ANDA
- Marketing start
- 2018-08-13
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7238-3 | 68788723803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7238-3) | 2018-08-13 | 0000-00-00 | No | No | Current |
| 68788-7238-6 | 68788723806 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7238-6) | 2018-08-13 | 0000-00-00 | No | No | Current |
| 68788-7238-9 | 68788723809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7238-9) | 2018-08-13 | 0000-00-00 | No | No | Current |