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CEFPROZIL
CEFPROZIL - 68180-404-02 - (CEFPROZIL)
Drug Information of CEFPROZIL
| Product NDC: | 68180-404 |
| Proprietary Name: | CEFPROZIL |
| Non Proprietary Name: | CEFPROZIL |
| Active Ingredient(s): | 500 mg/1 & nbsp; CEFPROZIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFPROZIL
| Product NDC: | 68180-404 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065276 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051201 |
Package Information of CEFPROZIL
| Package NDC: | 68180-404-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (68180-404-02) |
NDC Information of CEFPROZIL
| NDC Code | 68180-404-02 |
| Proprietary Name | CEFPROZIL |
| Package Description | 100 TABLET in 1 BOTTLE (68180-404-02) |
| Product NDC | 68180-404 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFPROZIL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051201 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | CEFPROZIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
