Generated: October 22, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 202139
, which is a drug marketed by Sun Pharm Inds, Glenmark Pharms Ltd, Sun Pharm Inds Inc, Zydus Pharms Usa Inc, Jubilant Generics, Parke Davis, Hetero Labs Ltd Iii, Inwood Labs, Cycle Pharms Ltd, Pioneer Pharms, Able, G And W Labs, Ivax Sub Teva Pharms, Mylan, Duramed Pharms Barr, Chartwell Rx, Chartwell Molecules, Watson Labs, Halsey, Fresenius Kabi Usa, Mylan Pharms Inc, Teva, Aurobindo Pharma Ltd, Pliva, Amneal Pharms, Heritage Pharms Inc, Novast Labs Ltd, Sandoz, Mutual Pharm, Watson Labs Inc, Avanthi Inc, Glenmark Generics, Superpharm, West-ward Pharms Int, Hospira Inc, and Navinta Llc, and is included in sixty-two NDAs. It is available from fifty-four suppliers. Additional details are available on the INDOMETHACIN profile page.
The generic ingredient in INDOMETHACIN is indomethacin sodium. There are fifteen drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the indomethacin sodium profile page.
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Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||CAPSULE, EXTENDED RELEASE;ORAL||Strength||75MG|
|Approval Date:||Mar 20, 2014||TE:||AB||RLD:||No|
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