Product NDC: | 54569-5917 |
Proprietary Name: | Cefdinir |
Non Proprietary Name: | Cefdinir |
Active Ingredient(s): | 250 mg/5mL & nbsp; Cefdinir |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-5917 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065429 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100806 |
Package NDC: | 54569-5917-0 |
Package Description: | 1 BOTTLE in 1 CARTON (54569-5917-0) > 60 mL in 1 BOTTLE |
NDC Code | 54569-5917-0 |
Proprietary Name | Cefdinir |
Package Description | 1 BOTTLE in 1 CARTON (54569-5917-0) > 60 mL in 1 BOTTLE |
Product NDC | 54569-5917 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cefdinir |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20100806 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | CEFDINIR MONOHYDRATE |
Strength Number | 250 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |