clopidogrel bisulfate
- Product NDC
- 60429-301
- 11-digit product format
- 604290301
- Labeler code
- 60429
- Product ID
- 60429-301_c59c681a-da6d-f028-e053-2995a90a549d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076274
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-301-10 | 60429030110 | 1000 TABLET, FILM COATED in 1 BOTTLE (60429-301-10) | 2012-05-23 | 0000-00-00 | No | No | Current |
| 60429-301-30 | 60429030130 | 30 TABLET, FILM COATED in 1 BOTTLE (60429-301-30) | 2012-05-23 | 0000-00-00 | No | No | Current |
| 60429-301-90 | 60429030190 | 90 TABLET, FILM COATED in 1 BOTTLE (60429-301-90) | 2012-05-23 | 0000-00-00 | No | No | Current |