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Erythrocin Stearate - 49349-790-50 - (ERYTHROMYCIN STEARATE)

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Drug Information of Erythrocin Stearate

Product NDC: 49349-790
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: 49349-790
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060359
Marketing Category: ANDA
Start Marketing Date: 20130305

Package Information of Erythrocin Stearate

Package NDC: 49349-790-50
Package Description: 40 TABLET, FILM COATED in 1 VIAL (49349-790-50)

NDC Information of Erythrocin Stearate

NDC Code 49349-790-50
Proprietary Name Erythrocin Stearate
Package Description 40 TABLET, FILM COATED in 1 VIAL (49349-790-50)
Product NDC 49349-790
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN STEARATE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130305
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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