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Ephedrine Sulfate - 66758-008-02 - (Ephedrine Sulfate)

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Drug Information of Ephedrine Sulfate

Product NDC: 66758-008
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ephedrine Sulfate

Product NDC: 66758-008
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20040326

Package Information of Ephedrine Sulfate

Package NDC: 66758-008-02
Package Description: 25 VIAL in 1 CARTON (66758-008-02) > 1 mL in 1 VIAL (66758-008-01)

NDC Information of Ephedrine Sulfate

NDC Code 66758-008-02
Proprietary Name Ephedrine Sulfate
Package Description 25 VIAL in 1 CARTON (66758-008-02) > 1 mL in 1 VIAL (66758-008-01)
Product NDC 66758-008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ephedrine Sulfate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20040326
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Sandoz Inc
Substance Name EPHEDRINE SULFATE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ephedrine Sulfate


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