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ERYTHROMYCIN Base Filmtab - 49999-012-40 - (ERYTHROMYCIN)

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Drug Information of ERYTHROMYCIN Base Filmtab

Product NDC: 49999-012
Proprietary Name: ERYTHROMYCIN Base Filmtab
Non Proprietary Name: ERYTHROMYCIN
Active Ingredient(s): 500    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 Filmtab

Product NDC: 49999-012
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061621
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of ERYTHROMYCIN Base Filmtab

Package NDC: 49999-012-40
Package Description: 40 TABLET, FILM COATED in 1 BOTTLE (49999-012-40)

NDC Information of ERYTHROMYCIN Base Filmtab

NDC Code 49999-012-40
Proprietary Name ERYTHROMYCIN Base Filmtab
Package Description 40 TABLET, FILM COATED in 1 BOTTLE (49999-012-40)
Product NDC 49999-012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ERYTHROMYCIN
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 ERYTHROMYCIN Base Filmtab


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