ZMAX - 0069-4170-02 - (azithromycin dihydrate)

Alphabetical Index


Drug Information of ZMAX

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)

Labeler Information of ZMAX

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 Information of ZMAX

Package NDC: 0069-4170-02
Package Description: 60 mL in 1 BOTTLE (0069-4170-02)

NDC Information of ZMAX

NDC Code 0069-4170-02
Proprietary Name ZMAX
Package Description 60 mL in 1 BOTTLE (0069-4170-02)
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]

Complete Information of ZMAX


General Information