INOmax - 64693-001-01 - (nitric oxide)

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Drug Information of INOmax

Product NDC: 64693-001
Proprietary Name: INOmax
Non Proprietary Name: nitric oxide
Active Ingredient(s): .123    mg/L & nbsp;   nitric oxide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): GAS
Coding System: National Drug Codes(NDC)

Labeler Information of INOmax

Product NDC: 64693-001
Labeler Name: INO Therapeutics
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020845
Marketing Category: NDA
Start Marketing Date: 19991223

Package Information of INOmax

Package NDC: 64693-001-01
Package Description: 1 CYLINDER in 1 CARTON (64693-001-01) > 344 L in 1 CYLINDER

NDC Information of INOmax

NDC Code 64693-001-01
Proprietary Name INOmax
Package Description 1 CYLINDER in 1 CARTON (64693-001-01) > 344 L in 1 CYLINDER
Product NDC 64693-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nitric oxide
Dosage Form Name GAS
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19991223
Marketing Category Name NDA
Labeler Name INO Therapeutics
Substance Name NITRIC OXIDE
Strength Number .123
Strength Unit mg/L
Pharmaceutical Classes Vasodilation [PE],Vasodilator [EPC]

Complete Information of INOmax


General Information