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Erythromycin Base - 52125-049-02 - (Erythromycin)

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Drug Information of Erythromycin Base

Product NDC: 52125-049
Proprietary Name: Erythromycin Base
Non Proprietary Name: Erythromycin
Active Ingredient(s): 250    mg/1 & nbsp;   Erythromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Erythromycin Base

Product NDC: 52125-049
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061621
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Erythromycin Base

Package NDC: 52125-049-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-049-02)

NDC Information of Erythromycin Base

NDC Code 52125-049-02
Proprietary Name Erythromycin Base
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-049-02)
Product NDC 52125-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Erythromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130314
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ERYTHROMYCIN
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 Erythromycin Base


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