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Indomethacin - 55390-299-01 - (Indomethacin)

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Drug Information of Indomethacin

Product NDC: 55390-299
Proprietary Name: Indomethacin
Non Proprietary Name: Indomethacin
Active Ingredient(s): .1    mg/.1mL & nbsp;   Indomethacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Indomethacin

Product NDC: 55390-299
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078713
Marketing Category: ANDA
Start Marketing Date: 20100211

Package Information of Indomethacin

Package NDC: 55390-299-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-299-01) > 1 mL in 1 VIAL

NDC Information of Indomethacin

NDC Code 55390-299-01
Proprietary Name Indomethacin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-299-01) > 1 mL in 1 VIAL
Product NDC 55390-299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Indomethacin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100211
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name INDOMETHACIN
Strength Number .1
Strength Unit mg/.1mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Indomethacin


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