Product NDC: | 60505-2616 |
Proprietary Name: | Clarithromycin |
Non Proprietary Name: | Clarithromycin |
Active Ingredient(s): | 250 mg/1 & nbsp; Clarithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-2616 |
Labeler Name: | Apotex Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065384 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070913 |
Package NDC: | 60505-2616-3 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (60505-2616-3) |
NDC Code | 60505-2616-3 |
Proprietary Name | Clarithromycin |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (60505-2616-3) |
Product NDC | 60505-2616 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clarithromycin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20070913 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp |
Substance Name | CLARITHROMYCIN |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |