Clopidogrel
- Product NDC
- 68071-4898
- 11-digit product format
- 680714898
- Labeler code
- 68071
- Product ID
- 68071-4898_bb917c5b-f8fe-55c5-e053-2a95a90ad45d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel bisulphate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202925
- Marketing category
- ANDA
- Marketing start
- 2013-11-21
- 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 |
|---|
| 68071-4898-3 | 68071489803 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4898-3) | 2019-05-17 | 0000-00-00 | No | No | Current |