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clarithromycin
clarithromycin - 62037-777-05 - (clarithromycin)
Drug Information of clarithromycin
| Product NDC: | 62037-777 |
| 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) |
Labeler Information of clarithromycin
| Product NDC: | 62037-777 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065145 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080101 |
Package Information of clarithromycin
| Package NDC: | 62037-777-05 |
| Package Description: | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-777-05) |
NDC Information of clarithromycin
| NDC Code | 62037-777-05 |
| Proprietary Name | clarithromycin |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-777-05) |
| Product NDC | 62037-777 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clarithromycin |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080101 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | CLARITHROMYCIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
