Clopidogrel
- Product NDC
- 50090-2598
- 11-digit product format
- 500902598
- Labeler code
- 50090
- Product ID
- 50090-2598_673d59c0-825f-4855-a2c5-6864e98e0925
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel bisulphate
- 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
- 2020-12-31
- 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 |
|---|
| 50090-2598 | CLOPIDOGREL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 12 | Legacy NDC | 20230208_21c99e1b-d370-4971-8f9c-d9d901db88fa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2598-0 | 50090259800 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2598-0) | 2016-11-04 | 0000-00-00 | No | No | Current |
| 50090-2598-1 | 50090259801 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2598-1) | 2016-11-07 | 0000-00-00 | No | No | Current |