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Erythrocin Stearate - 0074-6316-13 - (Erythromycin Stearate)

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Drug Information of Erythrocin Stearate

Product NDC: 0074-6316
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Erythrocin Stearate

Product NDC: 0074-6316
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060359
Marketing Category: ANDA
Start Marketing Date: 19640624

Package Information of Erythrocin Stearate

Package NDC: 0074-6316-13
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0074-6316-13)

NDC Information of Erythrocin Stearate

NDC Code 0074-6316-13
Proprietary Name Erythrocin Stearate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0074-6316-13)
Product NDC 0074-6316
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin Stearate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19640624
Marketing Category Name ANDA
Labeler Name Abbott Laboratories
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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