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CEFACLOR
CEFACLOR - 21695-782-15 - (CEFACLOR)
Drug Information of CEFACLOR
| Product NDC: | 21695-782 |
| Proprietary Name: | CEFACLOR |
| Non Proprietary Name: | CEFACLOR |
| Active Ingredient(s): | 250 mg/5mL & nbsp; CEFACLOR |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFACLOR
| Product NDC: | 21695-782 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064164 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19971002 |
Package Information of CEFACLOR
| Package NDC: | 21695-782-15 |
| Package Description: | 150 mL in 1 BOTTLE (21695-782-15) |
NDC Information of CEFACLOR
| NDC Code | 21695-782-15 |
| Proprietary Name | CEFACLOR |
| Package Description | 150 mL in 1 BOTTLE (21695-782-15) |
| Product NDC | 21695-782 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFACLOR |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19971002 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CEFACLOR |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
