Home
>
National Drug Code (NDC)
>
Cefaclor
Cefaclor - 63629-1305-5 - (Cefaclor)
Drug Information of Cefaclor
| Product NDC: | 63629-1305 |
| Proprietary Name: | Cefaclor |
| Non Proprietary Name: | Cefaclor |
| Active Ingredient(s): | 250 mg/1 & nbsp; Cefaclor |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefaclor
| Product NDC: | 63629-1305 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064156 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091106 |
Package Information of Cefaclor
| Package NDC: | 63629-1305-5 |
| Package Description: | 6 CAPSULE in 1 BOTTLE (63629-1305-5) |
NDC Information of Cefaclor
| NDC Code | 63629-1305-5 |
| Proprietary Name | Cefaclor |
| Package Description | 6 CAPSULE in 1 BOTTLE (63629-1305-5) |
| Product NDC | 63629-1305 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefaclor |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20091106 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | CEFACLOR |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
