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AZITHROMYCIN - 43063-090-02 - (AZITHROMYCIN)

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Drug Information of AZITHROMYCIN

Product NDC: 43063-090
Proprietary Name: AZITHROMYCIN
Non Proprietary Name: AZITHROMYCIN
Active Ingredient(s): 250    mg/1 & nbsp;   AZITHROMYCIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of AZITHROMYCIN

Product NDC: 43063-090
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065404
Marketing Category: ANDA
Start Marketing Date: 20080211

Package Information of AZITHROMYCIN

Package NDC: 43063-090-02
Package Description: 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-090-02)

NDC Information of AZITHROMYCIN

NDC Code 43063-090-02
Proprietary Name AZITHROMYCIN
Package Description 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-090-02)
Product NDC 43063-090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AZITHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080211
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name AZITHROMYCIN ANHYDROUS
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of AZITHROMYCIN


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