Clopidogrel
- Product NDC
- 72789-469
- 11-digit product format
- 727890469
- Labeler code
- 72789
- Product ID
- 72789-469_2abaa65e-cc80-156c-e063-6294a90a44be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090540
- Marketing category
- ANDA
- Marketing start
- 2012-05-17
- Substance
- CLOPIDOGREL BISULFATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72789-469-90 | 72789046990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-469-90) | 2025-01-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Clopidogrel | PD-Rx Pharmaceuticals, Inc. | 2025-01-02 | HUMAN PRESCRIPTION DRUG LABEL | 19 |