Product NDC: | 50063-003 |
Proprietary Name: | Air |
Non Proprietary Name: | Air |
Active Ingredient(s): | 1000 mL/L & nbsp; Air |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | GAS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50063-003 |
Labeler Name: | Andy-Oxy Co., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED MEDICAL GAS |
Start Marketing Date: | 20070101 |
Package NDC: | 50063-003-03 |
Package Description: | 1699 L in 1 CYLINDER (50063-003-03) |
NDC Code | 50063-003-03 |
Proprietary Name | Air |
Package Description | 1699 L in 1 CYLINDER (50063-003-03) |
Product NDC | 50063-003 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Air |
Dosage Form Name | GAS |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20070101 |
Marketing Category Name | UNAPPROVED MEDICAL GAS |
Labeler Name | Andy-Oxy Co., Inc. |
Substance Name | AIR |
Strength Number | 1000 |
Strength Unit | mL/L |
Pharmaceutical Classes |