Product NDC: | 54868-3384 |
Proprietary Name: | Biaxin |
Non Proprietary Name: | Clarithromycin |
Active Ingredient(s): | 250 mg/5mL & nbsp; Clarithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3384 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050698 |
Marketing Category: | NDA |
Start Marketing Date: | 20070501 |
Package NDC: | 54868-3384-0 |
Package Description: | 100 mL in 1 BOTTLE (54868-3384-0) |
NDC Code | 54868-3384-0 |
Proprietary Name | Biaxin |
Package Description | 100 mL in 1 BOTTLE (54868-3384-0) |
Product NDC | 54868-3384 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clarithromycin |
Dosage Form Name | GRANULE, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20070501 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CLARITHROMYCIN |
Strength Number | 250 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |