Product NDC: | 17478-515 |
Proprietary Name: | Ephedrine Sulfate |
Non Proprietary Name: | Ephedrine Sulfate |
Active Ingredient(s): | 50 mg/mL & nbsp; Ephedrine Sulfate |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-515 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090401 |
Package NDC: | 17478-515-00 |
Package Description: | 10 AMPULE in 1 CARTON (17478-515-00) > 1 mL in 1 AMPULE |
NDC Code | 17478-515-00 |
Proprietary Name | Ephedrine Sulfate |
Package Description | 10 AMPULE in 1 CARTON (17478-515-00) > 1 mL in 1 AMPULE |
Product NDC | 17478-515 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ephedrine Sulfate |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20090401 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Akorn, Inc. |
Substance Name | EPHEDRINE SULFATE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes |