Product NDC: | 54868-6348 |
Proprietary Name: | AZITHROMYCIN |
Non Proprietary Name: | AZITHROMYCIN |
Active Ingredient(s): | 600 mg/1 & nbsp; AZITHROMYCIN |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6348 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065302 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120426 |
Package NDC: | 54868-6348-0 |
Package Description: | 8 TABLET, FILM COATED in 1 BOTTLE (54868-6348-0) |
NDC Code | 54868-6348-0 |
Proprietary Name | AZITHROMYCIN |
Package Description | 8 TABLET, FILM COATED in 1 BOTTLE (54868-6348-0) |
Product NDC | 54868-6348 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | AZITHROMYCIN |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120426 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | AZITHROMYCIN ANHYDROUS |
Strength Number | 600 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |