Product NDC: | 46414-2222 |
Proprietary Name: | Amyl Nitrite |
Non Proprietary Name: | Amyl Nitrite |
Active Ingredient(s): | .3 g/.3mL & nbsp; Amyl Nitrite |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | INHALANT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 46414-2222 |
Labeler Name: | James Alexander Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19790207 |
Package NDC: | 46414-2222-8 |
Package Description: | 144 AMPULE in 1 CARTON (46414-2222-8) > .3 mL in 1 AMPULE (46414-2222-1) |
NDC Code | 46414-2222-8 |
Proprietary Name | Amyl Nitrite |
Package Description | 144 AMPULE in 1 CARTON (46414-2222-8) > .3 mL in 1 AMPULE (46414-2222-1) |
Product NDC | 46414-2222 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amyl Nitrite |
Dosage Form Name | INHALANT |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 19790207 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | James Alexander Corporation |
Substance Name | AMYL NITRITE |
Strength Number | .3 |
Strength Unit | g/.3mL |
Pharmaceutical Classes |