Product NDC: | 64693-002 |
Proprietary Name: | INOmax |
Non Proprietary Name: | nitric oxide |
Active Ingredient(s): | .98 mg/L & nbsp; nitric oxide |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | GAS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64693-002 |
Labeler Name: | INO Therapeutics |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020845 |
Marketing Category: | NDA |
Start Marketing Date: | 19991223 |
Package NDC: | 64693-002-01 |
Package Description: | 1 CYLINDER in 1 CARTON (64693-002-01) > 344 L in 1 CYLINDER |
NDC Code | 64693-002-01 |
Proprietary Name | INOmax |
Package Description | 1 CYLINDER in 1 CARTON (64693-002-01) > 344 L in 1 CYLINDER |
Product NDC | 64693-002 |
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 | .98 |
Strength Unit | mg/L |
Pharmaceutical Classes | Vasodilation [PE],Vasodilator [EPC] |