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Quinidine Gluconate - 53489-141-10 - (Quinidine Gluconate)

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Drug Information of Quinidine Gluconate

Product NDC: 53489-141
Proprietary Name: Quinidine Gluconate
Non Proprietary Name: Quinidine Gluconate
Active Ingredient(s): 324    mg/1 & nbsp;   Quinidine Gluconate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Quinidine Gluconate

Product NDC: 53489-141
Labeler Name: Mutual Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089338
Marketing Category: ANDA
Start Marketing Date: 19870210

Package Information of Quinidine Gluconate

Package NDC: 53489-141-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (53489-141-10)

NDC Information of Quinidine Gluconate

NDC Code 53489-141-10
Proprietary Name Quinidine Gluconate
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (53489-141-10)
Product NDC 53489-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinidine Gluconate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19870210
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical
Substance Name QUINIDINE GLUCONATE
Strength Number 324
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC],Cytochrome P450 2D6 Inhibitor [EPC],Cytochrome P450 2D6 Inhibitors [MoA]

Complete Information of Quinidine Gluconate


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