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Ephedrine Sulfate - 17478-515-00 - (Ephedrine Sulfate)

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Drug Information of Ephedrine Sulfate

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)

Labeler Information of Ephedrine Sulfate

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 Information of Ephedrine Sulfate

Package NDC: 17478-515-00
Package Description: 10 AMPULE in 1 CARTON (17478-515-00) > 1 mL in 1 AMPULE

NDC Information of Ephedrine Sulfate

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

Complete Information of Ephedrine Sulfate


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