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Amoxicillin
Amoxicillin - 0781-6039-55 - (Amoxicillin)
Drug Information of Amoxicillin
| Product NDC: | 0781-6039 |
| 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) |
Labeler Information of Amoxicillin
| Product NDC: | 0781-6039 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065387 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070326 |
Package Information of Amoxicillin
| Package NDC: | 0781-6039-55 |
| Package Description: | 150 mL in 1 BOTTLE (0781-6039-55) |
NDC Information of Amoxicillin
| NDC Code | 0781-6039-55 |
| Proprietary Name | Amoxicillin |
| Package Description | 150 mL in 1 BOTTLE (0781-6039-55) |
| Product NDC | 0781-6039 |
| 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 | Sandoz Inc |
| Substance Name | AMOXICILLIN |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
