Product NDC: | 54868-5648 |
Proprietary Name: | Azithromycin |
Non Proprietary Name: | azithromycin monohydrate |
Active Ingredient(s): | 200 mg/5mL & nbsp; azithromycin monohydrate |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5648 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA050710 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060803 |
Package NDC: | 54868-5648-2 |
Package Description: | 15 mL in 1 BOTTLE (54868-5648-2) |
NDC Code | 54868-5648-2 |
Proprietary Name | Azithromycin |
Package Description | 15 mL in 1 BOTTLE (54868-5648-2) |
Product NDC | 54868-5648 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azithromycin monohydrate |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20060803 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | AZITHROMYCIN |
Strength Number | 200 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |