clopidogrel
- Product NDC
- 70771-1062
- 11-digit product format
- 707711062
- Labeler code
- 70771
- Product ID
- 70771-1062_7f4e6a76-291d-4993-83c0-56877509cd56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA201686
- Marketing category
- ANDA
- Marketing start
- 2017-02-08
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1062 | CLOPIDOGREL TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED] | 7 | Legacy NDC | 20231005_3216ebb5-00ab-403d-98e6-36c5963b1a2c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1062-0 | 70771106200 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1062-0) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70771-1062-3 | 70771106203 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1062-3) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70771-1062-5 | 70771106205 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1062-5) | 2017-02-08 | 0000-00-00 | No | No | Current |
| 70771-1062-9 | 70771106209 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1062-9) | 2017-02-08 | 0000-00-00 | No | No | Current |