Clopidogrel
- Product NDC
- 70882-116
- 11-digit product format
- 708820116
- Labeler code
- 70882
- Product ID
- 70882-116_782ff485-7564-4446-8a45-4b121c59287c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clopidogrel bisulfate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA076274
- Marketing category
- ANDA
- Marketing start
- 2012-05-17
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70882-116-30 | Clopidogrel | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-116 | CLOPIDOGREL (CLOPIDOGREL BISULFATE) TABLET, FILM COATED [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Legacy NDC, 1 package rows | 20170310_944cfe97-75f3-4194-8a9b-b2a004bf4708.zip |
| 70882-116 | CLOPIDOGREL KIT KIT [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Legacy NDC | 20170801_126c5279-0ac1-4ed8-8c0f-b9084e3d7bb2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70882-116-30 | 70882011630 | 30 in 1 BLISTER PACK | Historical |