Product NDC: | 67253-145 |
Proprietary Name: | Amoxicillin |
Non Proprietary Name: | Amoxicillin |
Active Ingredient(s): | 875 mg/1 & nbsp; Amoxicillin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67253-145 |
Labeler Name: | DAVA International, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065344 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090715 |
Package NDC: | 67253-145-10 |
Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (67253-145-10) |
NDC Code | 67253-145-10 |
Proprietary Name | Amoxicillin |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (67253-145-10) |
Product NDC | 67253-145 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amoxicillin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20090715 |
Marketing Category Name | ANDA |
Labeler Name | DAVA International, Inc. |
Substance Name | AMOXICILLIN |
Strength Number | 875 |
Strength Unit | mg/1 |
Pharmaceutical Classes |