CLOPIDOGREL
- Product NDC
- 43547-485
- 11-digit product format
- 435470485
- Labeler code
- 43547
- Product ID
- 43547-485_ae9dcfd7-e402-4012-88e1-3e0de58a6514
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Solco Healthcare LLC
- Application
- ANDA206376
- Marketing category
- ANDA
- Marketing start
- 2018-07-10
- Marketing end
- 0000-00-00
- Substance
- CLOPIDOGREL BISULFATE
- Active strength
- 300 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43547-485-03 | 43547048503 | 30 TABLET in 1 BOTTLE (43547-485-03) | 30 tablet | 2018-07-10 | 0000-00-00 | No | No | Current |
| 43547-485-10 | 43547048510 | 100 TABLET in 1 BOTTLE (43547-485-10) | 100 tablet | 2018-07-10 | 0000-00-00 | No | No | Current |