Cefadroxil
- Product NDC
- 67296-1038
- 11-digit product format
- 672961038
- Labeler code
- 67296
- Product ID
- 67296-1038_d60f9a37-90c3-7879-e053-2995a90a4d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA065352
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- CEFADROXIL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 67296-1038-2 | Cefadroxil | 20 in 1 BOTTLE | CAPSULE | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1038 | CEFADROXIL CAPSULE [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220121_78ec0be1-b770-e670-e053-2991aa0af1e3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1038-2 | 67296103802 | 20 CAPSULE in 1 BOTTLE (67296-1038-2) | 20 capsule | 2018-01-01 | 0000-00-00 | No | No | Current |