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Indomethacin - 0185-0720-10 - (Indomethacin)

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Drug Information of Indomethacin

Product NDC: 0185-0720
Proprietary Name: Indomethacin
Non Proprietary Name: Indomethacin
Active Ingredient(s): 75    mg/1 & nbsp;   Indomethacin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Indomethacin

Product NDC: 0185-0720
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074464
Marketing Category: ANDA
Start Marketing Date: 19980528

Package Information of Indomethacin

Package NDC: 0185-0720-10
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0185-0720-10)

NDC Information of Indomethacin

NDC Code 0185-0720-10
Proprietary Name Indomethacin
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0185-0720-10)
Product NDC 0185-0720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Indomethacin
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19980528
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name INDOMETHACIN
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Indomethacin


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