Cefprozil
- Product NDC
- 0781-5043
- 11-digit product format
- 007815043
- Labeler code
- 0781
- Product ID
- 0781-5043_4272315e-8350-44d3-ab67-49488f766f61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefprozil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA065235
- Marketing category
- ANDA
- Marketing start
- 2005-11-14
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0781-5043-01 | EA - Each | 0781-5043 | 477ab2a6-bb3a-438a-b744-451cd6596d23 | 1 | 2013-02-11 |