Clopidogrel bisulfate
- Product NDC
- 70518-0717
- 11-digit product format
- 705180717
- Labeler code
- 70518
- Product ID
- 70518-0717_8c432a0f-06d2-3203-e053-2a95a90afe9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076273
- Marketing category
- ANDA
- Marketing start
- 2017-08-29
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0717 | CLOPIDOGREL BISULFATE TABLET, FILM COATED [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250429_893dbdc0-ff94-4246-a3ff-c542e6311d09.zip |