Clopidogrel
- Product NDC
- 50090-4918
- 11-digit product format
- 500904918
- Labeler code
- 50090
- Product ID
- 50090-4918_40a3f85b-4b48-4454-b0f0-a826e0f86466
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4918 | CLOPIDOGREL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC | 20230208_303d2e9f-3a8e-4965-a39a-032c5f31a431.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4918-0 | 50090491800 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4918-0) | 2020-02-18 | 0000-00-00 | No | No | Current |