Product NDC: | 17575-011 |
Proprietary Name: | Nitrous Oxide |
Non Proprietary Name: | Nitroux Oxide |
Active Ingredient(s): | 990 mL/L & nbsp; Nitroux Oxide |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | GAS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17575-011 |
Labeler Name: | AGL Inhalation Therapy Co. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED MEDICAL GAS |
Start Marketing Date: | 19660101 |
Package NDC: | 17575-011-06 |
Package Description: | 99792 L in 1 CYLINDER (17575-011-06) |
NDC Code | 17575-011-06 |
Proprietary Name | Nitrous Oxide |
Package Description | 99792 L in 1 CYLINDER (17575-011-06) |
Product NDC | 17575-011 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nitroux Oxide |
Dosage Form Name | GAS |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19660101 |
Marketing Category Name | UNAPPROVED MEDICAL GAS |
Labeler Name | AGL Inhalation Therapy Co. |
Substance Name | NITROUS OXIDE |
Strength Number | 990 |
Strength Unit | mL/L |
Pharmaceutical Classes |