Cefprozil
- Product NDC
- 0781-6203
- 11-digit product format
- 007816203
- Labeler code
- 0781
- Product ID
- 0781-6203_4272315e-8350-44d3-ab67-49488f766f61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefprozil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA065257
- Marketing category
- ANDA
- Marketing start
- 2005-12-05
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 250 mg/5mL
- 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 |
|---|---|---|---|---|---|
| 0781-6203-46 | ML - Milliliter | 0781-6203 | 2eb9ad78-4572-4af2-9840-1ce4ecb7a91c | 1 | 2013-02-13 |
| 0781-6203-57 | ML - Milliliter | 0781-6203 | c97a15a6-accc-4a6f-b39f-2a7eaffdc62b | 1 | 2013-02-13 |
| 0781-6203-91 | ML - Milliliter | 0781-6203 | c9a2fdb8-e662-47a3-851f-76423e16cd21 | 1 | 2013-02-13 |