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INDOMETHACIN - 0713-0176-30 - (INDOMETHACIN)

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Drug Information of INDOMETHACIN

Product NDC: 0713-0176
Proprietary Name: INDOMETHACIN
Non Proprietary Name: INDOMETHACIN
Active Ingredient(s): 50    mg/1 & nbsp;   INDOMETHACIN
Administration Route(s): RECTAL
Dosage Form(s): SUPPOSITORY
Coding System: National Drug Codes(NDC)

Labeler Information of INDOMETHACIN

Product NDC: 0713-0176
Labeler Name: G & W LABORATORIES, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073314
Marketing Category: ANDA
Start Marketing Date: 19920831

Package Information of INDOMETHACIN

Package NDC: 0713-0176-30
Package Description: 30 SUPPOSITORY in 1 BOX (0713-0176-30)

NDC Information of INDOMETHACIN

NDC Code 0713-0176-30
Proprietary Name INDOMETHACIN
Package Description 30 SUPPOSITORY in 1 BOX (0713-0176-30)
Product NDC 0713-0176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name INDOMETHACIN
Dosage Form Name SUPPOSITORY
Route Name RECTAL
Start Marketing Date 19920831
Marketing Category Name ANDA
Labeler Name G & W LABORATORIES, INC.
Substance Name INDOMETHACIN
Strength Number 50
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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