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Cefaclor
Cefaclor - 0093-1087-01 - (Cefaclor)
Drug Information of Cefaclor
| Product NDC: | 0093-1087 |
| Proprietary Name: | Cefaclor |
| Non Proprietary Name: | Cefaclor |
| Active Ingredient(s): | 500 mg/1 & nbsp; Cefaclor |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefaclor
| Product NDC: | 0093-1087 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065058 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020926 |
Package Information of Cefaclor
| Package NDC: | 0093-1087-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1087-01) |
NDC Information of Cefaclor
| NDC Code | 0093-1087-01 |
| Proprietary Name | Cefaclor |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-1087-01) |
| Product NDC | 0093-1087 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefaclor |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20020926 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | CEFACLOR |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
