CEFPROZIL
- Product NDC
- 53217-031
- 11-digit product format
- 532170031
- Labeler code
- 53217
- Product ID
- 53217-031_6ef123b8-910d-4715-986f-011aa8f4fcc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFPROZIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA065276
- Marketing category
- ANDA
- Marketing start
- 2005-12-01
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 500 mg/1
- 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 |
|---|
| 53217-031-20 | CEFPROZIL | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-031 | CEFPROZIL TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20170309_f6c29d0f-c00e-44c9-a7e6-70ad143bb564.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-031-20 | 53217003120 | 20 in 1 BOTTLE | Historical |