Ephedrine - 0409-3073-31 - (EPHEDRINE SULFATE)

Alphabetical Index


Drug Information of Ephedrine

Product NDC: 0409-3073
Proprietary Name: Ephedrine
Non Proprietary Name: EPHEDRINE SULFATE
Active Ingredient(s): 50    mg/mL & nbsp;   EPHEDRINE SULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ephedrine

Product NDC: 0409-3073
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050908

Package Information of Ephedrine

Package NDC: 0409-3073-31
Package Description: 10 AMPULE in 1 CARTON (0409-3073-31) > 1 mL in 1 AMPULE

NDC Information of Ephedrine

NDC Code 0409-3073-31
Proprietary Name Ephedrine
Package Description 10 AMPULE in 1 CARTON (0409-3073-31) > 1 mL in 1 AMPULE
Product NDC 0409-3073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EPHEDRINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20050908
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name EPHEDRINE SULFATE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ephedrine


General Information