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ERYTHROMYCIN - 16590-091-30 - (ERYTHROMYCIN)

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Drug Information of ERYTHROMYCIN

Product NDC: 16590-091
Proprietary Name: ERYTHROMYCIN
Non Proprietary Name: ERYTHROMYCIN
Active Ingredient(s): 250    mg/1 & nbsp;   ERYTHROMYCIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ERYTHROMYCIN

Product NDC: 16590-091
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061621
Marketing Category: ANDA
Start Marketing Date: 19720711

Package Information of ERYTHROMYCIN

Package NDC: 16590-091-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-091-30)

NDC Information of ERYTHROMYCIN

NDC Code 16590-091-30
Proprietary Name ERYTHROMYCIN
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-091-30)
Product NDC 16590-091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19720711
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name ERYTHROMYCIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of ERYTHROMYCIN


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