Cefprozil
- Product NDC
- 42043-262
- 11-digit product format
- 420430262
- Labeler code
- 42043
- Product ID
- 42043-262_0adde9cc-25aa-4535-acb3-f1e73825933c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefprozil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- OrchidPharma Inc
- Application
- ANDA065284
- Marketing category
- ANDA
- Marketing start
- 2015-08-19
- Marketing end
- 2019-11-30
- Substance
- CEFPROZIL
- Active strength
- 125 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record