CEFPROZIL
- Product NDC
- 67296-0590
- 11-digit product format
- 672960590
- Labeler code
- 67296
- Product ID
- 67296-0590_f4127116-3810-414d-9acf-ddb8e16fffbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFPROZIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA065276
- Marketing category
- ANDA
- Marketing start
- 2005-12-08
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67296-0590-1 | CEFPROZIL | 20 in 1 BOTTLE | TABLET | 20 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0590 | CEFPROZIL TABLET [REDPHARM DRUG INC.] | 2 | Legacy NDC, 1 package rows | 20110708_0f96e4fe-8daf-492b-8fd8-90ff25243077.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0590-1 | 67296059001 | 20 in 1 BOTTLE | Historical |