Clopidogrel
- Product NDC
- 71335-1409
- 11-digit product format
- 713351409
- Labeler code
- 71335
- Product ID
- 71335-1409_1c5aa3bf-7999-4b7c-ac52-3d0f80b4240d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1409-1 | 71335140901 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1409-1) | 2019-11-22 | 0000-00-00 | No | No | Current |
| 71335-1409-2 | 71335140902 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1409-2) | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1409-3 | 71335140903 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1409-3) | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1409-4 | 71335140904 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1409-4) | 2022-02-14 | 0000-00-00 | No | No | Current |
| 71335-1409-5 | 71335140905 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1409-5) | 2022-02-14 | 0000-00-00 | No | No | Current |