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Cosyntropin - 67457-257-02 - (cosyntropin)

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Drug Information of Cosyntropin

Product NDC: 67457-257
Proprietary Name: Cosyntropin
Non Proprietary Name: cosyntropin
Active Ingredient(s): .25    mg/mL & nbsp;   cosyntropin
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cosyntropin

Product NDC: 67457-257
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090574
Marketing Category: ANDA
Start Marketing Date: 20130508

Package Information of Cosyntropin

Package NDC: 67457-257-02
Package Description: 10 VIAL in 1 CARTON (67457-257-02) > 1 mL in 1 VIAL (67457-257-00)

NDC Information of Cosyntropin

NDC Code 67457-257-02
Proprietary Name Cosyntropin
Package Description 10 VIAL in 1 CARTON (67457-257-02) > 1 mL in 1 VIAL (67457-257-00)
Product NDC 67457-257
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cosyntropin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20130508
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name COSYNTROPIN
Strength Number .25
Strength Unit mg/mL
Pharmaceutical Classes Adrenocorticotropic Hormone [Chemical/Ingredient],Adrenocorticotropic Hormone [EPC]

Complete Information of Cosyntropin


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