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Indomethacin - 49349-873-20 - (Indomethacin)

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Drug Information of Indomethacin

Product NDC: 49349-873
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: 49349-873
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091549
Marketing Category: ANDA
Start Marketing Date: 20120301

Package Information of Indomethacin

Package NDC: 49349-873-20
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 CANISTER (49349-873-20)

NDC Information of Indomethacin

NDC Code 49349-873-20
Proprietary Name Indomethacin
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 CANISTER (49349-873-20)
Product NDC 49349-873
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Indomethacin
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120301
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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