Clopidogrel
- Product NDC
- 70786-0060
- 11-digit product format
- 707860060
- Labeler code
- 70786
- Product ID
- 70786-0060_3abff4b7-841e-4f9b-9c45-9aac10141419
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA202928
- Marketing category
- ANDA
- Marketing start
- 2012-10-16
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70786-0060-1 | Clopidogrel | 30 in 1 BOTTLE | TABLET | 30 | | 5 |
| 70786-0060-3 | Clopidogrel | 90 in 1 BOTTLE | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70786-0060 | CLOPIDOGREL TABLET [UNIT DOSE SERVICES] | 5 | Legacy NDC, 2 package rows | 20171108_5b0caa99-c313-4b39-a6ad-df662823e343.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70786-0060-1 | 70786006001 | 30 in 1 BOTTLE | Historical |
| 70786-0060-3 | 70786006003 | 90 in 1 BOTTLE | Historical |