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Cefprozil
Cefprozil - 16714-209-01 - (Cefprozil)
Drug Information of Cefprozil
| Product NDC: | 16714-209 |
| Proprietary Name: | Cefprozil |
| Non Proprietary Name: | Cefprozil |
| Active Ingredient(s): | 500 mg/1 & nbsp; Cefprozil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefprozil
| Product NDC: | 16714-209 |
| Labeler Name: | Northstar Rx LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065267 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070723 |
Package Information of Cefprozil
| Package NDC: | 16714-209-01 |
| Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-209-01) |
NDC Information of Cefprozil
| NDC Code | 16714-209-01 |
| Proprietary Name | Cefprozil |
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-209-01) |
| Product NDC | 16714-209 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefprozil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070723 |
| Marketing Category Name | ANDA |
| Labeler Name | Northstar Rx LLC |
| Substance Name | CEFPROZIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
