Product NDC: | 65862-501 |
Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Non Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Active Ingredient(s): | 250; 125 mg/1; mg/1 & nbsp; Amoxicillin and Clavulanate Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65862-501 |
Labeler Name: | Aurobindo Pharma Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091569 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120120 |
Package NDC: | 65862-501-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (65862-501-30) |
NDC Code | 65862-501-30 |
Proprietary Name | Amoxicillin and Clavulanate Potassium |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (65862-501-30) |
Product NDC | 65862-501 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amoxicillin and Clavulanate Potassium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120120 |
Marketing Category Name | ANDA |
Labeler Name | Aurobindo Pharma Limited |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength Number | 250; 125 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |