clopidogrel
- Product NDC
- 70710-1417
- 11-digit product format
- 707101417
- Labeler code
- 70710
- Product ID
- 70710-1417_21a4e2a5-f416-4438-8602-9582a5dcb102
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA201686
- Marketing category
- ANDA
- Marketing start
- 2017-02-08
- 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 |
|---|
| 70710-1417-0 | 70710141700 | 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1417-0) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70710-1417-3 | 70710141703 | 30 TABLET, FILM COATED in 1 BOTTLE (70710-1417-3) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70710-1417-5 | 70710141705 | 500 TABLET, FILM COATED in 1 BOTTLE (70710-1417-5) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70710-1417-9 | 70710141709 | 90 TABLET, FILM COATED in 1 BOTTLE (70710-1417-9) | 2017-02-08 | 0000-00-00 | No | No | Current |