Product NDC: | 0069-4170 |
Proprietary Name: | ZMAX |
Non Proprietary Name: | azithromycin dihydrate |
Active Ingredient(s): | 2 g/60mL & nbsp; azithromycin dihydrate |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0069-4170 |
Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050797 |
Marketing Category: | NDA |
Start Marketing Date: | 19950610 |
Package NDC: | 0069-4170-34 |
Package Description: | 60 mL in 1 BOTTLE (0069-4170-34) |
NDC Code | 0069-4170-34 |
Proprietary Name | ZMAX |
Package Description | 60 mL in 1 BOTTLE (0069-4170-34) |
Product NDC | 0069-4170 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azithromycin dihydrate |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19950610 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Laboratories Div Pfizer Inc |
Substance Name | AZITHROMYCIN DIHYDRATE |
Strength Number | 2 |
Strength Unit | g/60mL |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |