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Quinidine Sulfate - 0185-4346-01 - (Quinidine Sulfate)

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Drug Information of Quinidine Sulfate

Product NDC: 0185-4346
Proprietary Name: Quinidine Sulfate
Non Proprietary Name: Quinidine Sulfate
Active Ingredient(s): 200    mg/1 & nbsp;   Quinidine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Quinidine Sulfate

Product NDC: 0185-4346
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088072
Marketing Category: ANDA
Start Marketing Date: 19761124

Package Information of Quinidine Sulfate

Package NDC: 0185-4346-01
Package Description: 100 TABLET in 1 BOTTLE (0185-4346-01)

NDC Information of Quinidine Sulfate

NDC Code 0185-4346-01
Proprietary Name Quinidine Sulfate
Package Description 100 TABLET in 1 BOTTLE (0185-4346-01)
Product NDC 0185-4346
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinidine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19761124
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name QUINIDINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antiarrhythmic [EPC],Cytochrome P450 2D6 Inhibitor [EPC],Cytochrome P450 2D6 Inhibitors [MoA]

Complete Information of Quinidine Sulfate


General Information