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Indomethacin - 10702-016-10 - (Indomethacin)

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Drug Information of Indomethacin

Product NDC: 10702-016
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: 10702-016
Labeler Name: KVK-Tech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079175
Marketing Category: ANDA
Start Marketing Date: 20120727

Package Information of Indomethacin

Package NDC: 10702-016-10
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10702-016-10)

NDC Information of Indomethacin

NDC Code 10702-016-10
Proprietary Name Indomethacin
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10702-016-10)
Product NDC 10702-016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Indomethacin
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120727
Marketing Category Name ANDA
Labeler Name KVK-Tech, 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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