Clopidogrel Bisulfate
- Product NDC
- 68071-4268
- 11-digit product format
- 680714268
- Labeler code
- 68071
- Product ID
- 68071-4268_bb78a694-048d-6685-e053-2a95a90a51e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090494
- Marketing category
- ANDA
- Marketing start
- 2012-05-18
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4268-9 | 68071426809 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4268-9) | 2018-02-06 | 0000-00-00 | No | No | Current |