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Ergoloid Mesylates - 53489-281-10 - (Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate)

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Drug Information of Ergoloid Mesylates

Product NDC: 53489-281
Proprietary Name: Ergoloid Mesylates
Non Proprietary Name: Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate
Active Ingredient(s): .222; .111; .333; .333    mg/1; mg/1; mg/1; mg/1 & nbsp;   Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ergoloid Mesylates

Product NDC: 53489-281
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081113
Marketing Category: ANDA
Start Marketing Date: 19911031

Package Information of Ergoloid Mesylates

Package NDC: 53489-281-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (53489-281-10)

NDC Information of Ergoloid Mesylates

NDC Code 53489-281-10
Proprietary Name Ergoloid Mesylates
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (53489-281-10)
Product NDC 53489-281
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19911031
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name DIHYDRO-.ALPHA.-ERGOCRYPTINE MESYLATE; DIHYDRO-.BETA.-ERGOCRYPTINE MESYLATE; DIHYDROERGOCORNINE MESYLATE; DIHYDROERGOCRISTINE MESYLATE
Strength Number .222; .111; .333; .333
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ergoloid Mesylates


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