Clopidogrel Kit
- Product NDC
- 70882-123
- 11-digit product format
- 708820123
- Labeler code
- 70882
- Product ID
- 70882-123_126c5279-0ac1-4ed8-8c0f-b9084e3d7bb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel Kit
- Dosage form
- KIT
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA076274
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 |
|---|
| 70882-122-30 | Clopidogrel Kit | 30 in 1 BLISTER PACK | TABLET, COATED | 30 | 81 mg | 1 |
| 70882-123-01 | Clopidogrel Kit | 1 in 1 KIT | KIT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-123 | CLOPIDOGREL KIT KIT [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 1 | Legacy NDC, 2 package rows | 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 |
|---|
| 70882-122-30 | 70882012230 | 30 in 1 BLISTER PACK | Historical |
| 70882-123-01 | 70882012301 | 1 in 1 KIT | Historical |