Product NDC: | 54569-2930 |
Proprietary Name: | Amoxicillin |
Non Proprietary Name: | Amoxicillin |
Active Ingredient(s): | 125 mg/5mL & nbsp; Amoxicillin |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-2930 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065387 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070326 |
Package NDC: | 54569-2930-0 |
Package Description: | 150 mL in 1 BOTTLE (54569-2930-0) |
NDC Code | 54569-2930-0 |
Proprietary Name | Amoxicillin |
Package Description | 150 mL in 1 BOTTLE (54569-2930-0) |
Product NDC | 54569-2930 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amoxicillin |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20070326 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | AMOXICILLIN |
Strength Number | 125 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |