Clopidogrel
- Product NDC
- 70934-708
- 11-digit product format
- 709340708
- Labeler code
- 70934
- Product ID
- 70934-708_a9dea7d0-ea8a-8b93-e053-2995a90a345a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA202925
- Marketing category
- ANDA
- Marketing start
- 2020-06-16
- 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 |
|---|
| 70934-708-30 | 70934070830 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-708-30) | 2020-08-17 | 0000-00-00 | No | No | Current |
| 70934-708-90 | 70934070890 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-708-90) | 2020-06-16 | 0000-00-00 | No | No | Current |