Product NDC: | 68382-763 |
Proprietary Name: | Clarithromycin |
Non Proprietary Name: | Clarithromycin |
Active Ingredient(s): | 500 mg/1 & nbsp; Clarithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68382-763 |
Labeler Name: | Zydus Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050775 |
Marketing Category: | NDA |
Start Marketing Date: | 20000303 |
Package NDC: | 68382-763-14 |
Package Description: | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-763-14) |
NDC Code | 68382-763-14 |
Proprietary Name | Clarithromycin |
Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-763-14) |
Product NDC | 68382-763 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clarithromycin |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20000303 |
Marketing Category Name | NDA |
Labeler Name | Zydus Pharmaceuticals USA Inc |
Substance Name | CLARITHROMYCIN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |