Product NDC: | 0054-0036 |
Proprietary Name: | Clarithromycin |
Non Proprietary Name: | clarithromycin |
Active Ingredient(s): | 250 mg/1 & nbsp; clarithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-0036 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065178 |
Marketing Category: | ANDA |
Start Marketing Date: | 20041122 |
Package NDC: | 0054-0036-21 |
Package Description: | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (0054-0036-21) |
NDC Code | 0054-0036-21 |
Proprietary Name | Clarithromycin |
Package Description | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (0054-0036-21) |
Product NDC | 0054-0036 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clarithromycin |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20041122 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | CLARITHROMYCIN |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |