Cefprozil
- Product NDC
- 67253-231
- 11-digit product format
- 672530231
- Labeler code
- 67253
- Product ID
- 67253-231_f955de50-1f07-4079-9c2c-bd23ef54fd70
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefprozil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DAVA Pharmaceuticals Inc
- Application
- ANDA065235
- Marketing category
- ANDA
- Marketing start
- 2014-08-01
- Marketing end
- 2020-10-31
- Substance
- CEFPROZIL
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record