Cefprozil
- Product NDC
- 50090-1739
- 11-digit product format
- 500901739
- Labeler code
- 50090
- Product ID
- 50090-1739_84dfe213-8bd1-4c33-90d7-fc62402968aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefprozil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065340
- Marketing category
- ANDA
- Marketing start
- 2007-05-24
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 500 mg/1
- 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 |
|---|
| 50090-1739-0 | Cefprozil | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1739 | CEFPROZIL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 1 package rows | 20201030_1c924c12-fa53-42a1-bab9-f4daf435c466.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1739-0 | 50090173900 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-1739-0) | 2015-03-11 | 0000-00-00 | No | No | Current |