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Erythrocin Stearate - 55289-112-15 - (ERYTHROMYCIN STEARATE)

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Drug Information of Erythrocin Stearate

Product NDC: 55289-112
Proprietary Name: Erythrocin Stearate
Non Proprietary Name: ERYTHROMYCIN STEARATE
Active Ingredient(s): 250    mg/1 & nbsp;   ERYTHROMYCIN STEARATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Erythrocin Stearate

Product NDC: 55289-112
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060359
Marketing Category: ANDA
Start Marketing Date: 20110801

Package Information of Erythrocin Stearate

Package NDC: 55289-112-15
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-112-15)

NDC Information of Erythrocin Stearate

NDC Code 55289-112-15
Proprietary Name Erythrocin Stearate
Package Description 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-112-15)
Product NDC 55289-112
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN STEARATE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ERYTHROMYCIN STEARATE
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 Erythrocin Stearate


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