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Quinidine Gluconate - 0002-1407-01 - (Quinidine Gluconate)

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Drug Information of Quinidine Gluconate

Product NDC: 0002-1407
Proprietary Name: Quinidine Gluconate
Non Proprietary Name: Quinidine Gluconate
Active Ingredient(s): 80    mg/mL & nbsp;   Quinidine Gluconate
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Quinidine Gluconate

Product NDC: 0002-1407
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA007529
Marketing Category: NDA
Start Marketing Date: 19510301

Package Information of Quinidine Gluconate

Package NDC: 0002-1407-01
Package Description: 10 mL in 1 VIAL (0002-1407-01)

NDC Information of Quinidine Gluconate

NDC Code 0002-1407-01
Proprietary Name Quinidine Gluconate
Package Description 10 mL in 1 VIAL (0002-1407-01)
Product NDC 0002-1407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quinidine Gluconate
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19510301
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name QUINIDINE GLUCONATE
Strength Number 80
Strength Unit mg/mL
Pharmaceutical Classes Antiarrhythmic [EPC],Cytochrome P450 2D6 Inhibitor [EPC],Cytochrome P450 2D6 Inhibitors [MoA]

Complete Information of Quinidine Gluconate


General Information