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Erythrocin Stearate - 24236-360-06 - (ERYTHROMYCIN STEARATE)

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Drug Information of Erythrocin Stearate

Product NDC: 24236-360
Proprietary Name: Erythrocin Stearate
Non Proprietary Name: ERYTHROMYCIN STEARATE
Active Ingredient(s): 500    mg/1 & nbsp;   ERYTHROMYCIN STEARATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Erythrocin Stearate

Product NDC: 24236-360
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060359
Marketing Category: ANDA
Start Marketing Date: 20120827

Package Information of Erythrocin Stearate

Package NDC: 24236-360-06
Package Description: 28 TABLET in 1 BLISTER PACK (24236-360-06)

NDC Information of Erythrocin Stearate

NDC Code 24236-360-06
Proprietary Name Erythrocin Stearate
Package Description 28 TABLET in 1 BLISTER PACK (24236-360-06)
Product NDC 24236-360
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN STEARATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120827
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ERYTHROMYCIN STEARATE
Strength Number 500
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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