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Cefadroxil
Cefadroxil - 54868-5694-0 - (cefadroxil monohydrate)
Drug Information of Cefadroxil
| Product NDC: | 54868-5694 |
| Proprietary Name: | Cefadroxil |
| Non Proprietary Name: | cefadroxil monohydrate |
| Active Ingredient(s): | 500 mg/5mL & nbsp; cefadroxil monohydrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefadroxil
| Product NDC: | 54868-5694 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065115 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070516 |
Package Information of Cefadroxil
| Package NDC: | 54868-5694-0 |
| Package Description: | 100 mL in 1 BOTTLE (54868-5694-0) |
NDC Information of Cefadroxil
| NDC Code | 54868-5694-0 |
| Proprietary Name | Cefadroxil |
| Package Description | 100 mL in 1 BOTTLE (54868-5694-0) |
| Product NDC | 54868-5694 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefadroxil monohydrate |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20070516 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CEFADROXIL |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
