Cefprozil
- Product NDC
- 0781-6202
- 11-digit product format
- 007816202
- Labeler code
- 0781
- Product ID
- 0781-6202_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
- 125 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 |
|---|---|---|---|---|---|
| 0781-6202-46 | ML - Milliliter | 0781-6202 | 34900fec-65e7-4bd6-86d7-fd0687373ded | 1 | 2013-02-13 |
| 0781-6202-57 | ML - Milliliter | 0781-6202 | 280af0b6-4a1a-4f0e-b9ac-58974625eebe | 1 | 2013-02-13 |
| 0781-6202-91 | ML - Milliliter | 0781-6202 | 680448a4-8161-44ec-977c-08d8b8ee3131 | 1 | 2013-02-13 |