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CEFACLOR
CEFACLOR - 43063-194-30 - (CEFACLOR)
Drug Information of CEFACLOR
| Product NDC: | 43063-194 |
| Proprietary Name: | CEFACLOR |
| Non Proprietary Name: | CEFACLOR |
| Active Ingredient(s): | 500 mg/1 & nbsp; CEFACLOR |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFACLOR
| Product NDC: | 43063-194 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065350 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070501 |
Package Information of CEFACLOR
| Package NDC: | 43063-194-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-194-30) |
NDC Information of CEFACLOR
| NDC Code | 43063-194-30 |
| Proprietary Name | CEFACLOR |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-194-30) |
| Product NDC | 43063-194 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFACLOR |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070501 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | CEFACLOR |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
