Cefadroxil
- Product NDC
- 53002-2290
- 11-digit product format
- 530022290
- Labeler code
- 53002
- Product ID
- 53002-2290_8f0522ba-647e-49bb-a79a-d5126be64849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA065392
- Marketing category
- ANDA
- Marketing start
- 2008-04-23
- 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
- 2021-12-31
- 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 |
|---|
| 53002-2290-2 | Cefadroxil | 100 in 1 BOTTLE | CAPSULE | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53002-2290 | CEFADROXIL CAPSULE [RPK PHARMACEUTICALS, INC.] | 5 | Legacy NDC, 1 package rows | 20230609_eddf5ff1-4e3b-40e7-b037-df034f57f9f6.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 |
|---|
| 53002-2290-2 | 53002229002 | 100 CAPSULE in 1 BOTTLE (53002-2290-2) | 100 capsule | 2018-10-01 | 0000-00-00 | No | No | Current |