INDOCIN - 42211-101-01 - (indomethacin)

Alphabetical Index


Drug Information of INDOCIN

Product NDC: 42211-101
Proprietary Name: INDOCIN
Non Proprietary Name: indomethacin
Active Ingredient(s): 25    mg/5mL & nbsp;   indomethacin
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of INDOCIN

Product NDC: 42211-101
Labeler Name: Iroko Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018332
Marketing Category: NDA
Start Marketing Date: 19851010

Package Information of INDOCIN

Package NDC: 42211-101-01
Package Description: 1 BOTTLE in 1 CARTON (42211-101-01) > 50 mL in 1 BOTTLE

NDC Information of INDOCIN

NDC Code 42211-101-01
Proprietary Name INDOCIN
Package Description 1 BOTTLE in 1 CARTON (42211-101-01) > 50 mL in 1 BOTTLE
Product NDC 42211-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name indomethacin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19851010
Marketing Category Name NDA
Labeler Name Iroko Pharmaceuticals, LLC
Substance Name INDOMETHACIN
Strength Number 25
Strength Unit mg/5mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of INDOCIN


General Information