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Cefaclor
Cefaclor - 16571-070-12 - (Cefaclor)
Drug Information of Cefaclor
| Product NDC: | 16571-070 |
| Proprietary Name: | Cefaclor |
| Non Proprietary Name: | Cefaclor |
| Active Ingredient(s): | 125 mg/5mL & nbsp; Cefaclor |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefaclor
| Product NDC: | 16571-070 |
| Labeler Name: | Pack Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065412 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121025 |
Package Information of Cefaclor
| Package NDC: | 16571-070-12 |
| Package Description: | 150 mL in 1 BOTTLE (16571-070-12) |
NDC Information of Cefaclor
| NDC Code | 16571-070-12 |
| Proprietary Name | Cefaclor |
| Package Description | 150 mL in 1 BOTTLE (16571-070-12) |
| Product NDC | 16571-070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefaclor |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20121025 |
| Marketing Category Name | ANDA |
| Labeler Name | Pack Pharmaceuticals, LLC |
| Substance Name | CEFACLOR |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
