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ERYTHROMYCIN Base Filmtab - 21695-389-30 - (ERYTHROMYCIN)

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Drug Information of ERYTHROMYCIN Base Filmtab

Product NDC: 21695-389
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: 21695-389
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061621
Marketing Category: ANDA
Start Marketing Date: 19720711

Package Information of ERYTHROMYCIN Base Filmtab

Package NDC: 21695-389-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-389-30)

NDC Information of ERYTHROMYCIN Base Filmtab

NDC Code 21695-389-30
Proprietary Name ERYTHROMYCIN Base Filmtab
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-389-30)
Product NDC 21695-389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ERYTHROMYCIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19720711
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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