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Erythromycin - 24208-910-19 - (Erythromycin)

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Drug Information of Erythromycin

Product NDC: 24208-910
Proprietary Name: Erythromycin
Non Proprietary Name: Erythromycin
Active Ingredient(s): 5    mg/g & nbsp;   Erythromycin
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Erythromycin

Product NDC: 24208-910
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064067
Marketing Category: ANDA
Start Marketing Date: 19940729

Package Information of Erythromycin

Package NDC: 24208-910-19
Package Description: 50 TUBE in 1 BOX (24208-910-19) > 1 g in 1 TUBE

NDC Information of Erythromycin

NDC Code 24208-910-19
Proprietary Name Erythromycin
Package Description 50 TUBE in 1 BOX (24208-910-19) > 1 g in 1 TUBE
Product NDC 24208-910
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin
Dosage Form Name OINTMENT
Route Name OPHTHALMIC
Start Marketing Date 19940729
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
Substance Name ERYTHROMYCIN
Strength Number 5
Strength Unit mg/g
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient]

Complete Information of Erythromycin


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