CEFPROZIL
- Product NDC
- 43063-842
- 11-digit product format
- 430630842
- Labeler code
- 43063
- Product ID
- 43063-842_7cd7c4c0-e6cf-98eb-e053-2991aa0ab231
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CEFPROZIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA065276
- Marketing category
- ANDA
- Marketing start
- 2005-12-01
- Marketing end
- 0000-00-00
- Substance
- CEFPROZIL
- Active strength
- 500 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 |
|---|---|---|---|---|---|
| 43063-842-20 | EA - Each | 43063-842 | 2baca1d2-e7a1-4de8-aa53-7bc29896c1bc | 1 | 2018-04-19 |