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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 202711

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NDA 202711 describes INDOMETHACIN, which is a drug marketed by Able, Amneal Pharms, Aurobindo Pharma, Avanthi Inc, Chartwell Rx, Glenmark Pharms Ltd, Hetero Labs Ltd Iii, Inwood Labs, Jubilant Generics, Mylan, Novast Labs, Sandoz, Watson Labs Inc, Zydus Pharms, Ani Pharms, Chartwell Molecules, Cycle, Duramed Pharms Barr, Halsey, Heritage, Heritage Pharma, Ivax Sub Teva Pharms, Mutual Pharm, Parke Davis, Pioneer Pharms, Rising, Sun Pharm Inds Inc, Sun Pharm Industries, Superpharm, Teva, Watson Labs, Zydus Lifesciences, Fresenius Kabi Usa, Cosette, Hikma, Novitium Pharma, Hospira, Navinta Llc, and West-ward Pharms Int, and is included in sixty-four NDAs. It is available from thirty-two 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. Additional details are available on the indomethacin sodium profile page.

Summary for 202711

Tradename:	INDOMETHACIN
Applicant:	Zydus Pharms
Ingredient:	indomethacin
Patents:	0

Pharmacology for NDA: 202711

Mechanism of Action	Cyclooxygenase Inhibitors

Medical Subject Heading (MeSH) Categories for 202711

Anti-Inflammatory Agents, Non-Steroidal
Cardiovascular Agents
Cyclooxygenase Inhibitors
Gout Suppressants
Tocolytic Agents

Suppliers and Packaging for NDA: 202711

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
INDOMETHACIN	indomethacin	CAPSULE, EXTENDED RELEASE;ORAL	202711	ANDA	Zydus Pharmaceuticals USA Inc.	68382-371	68382-371-01	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-371-01)
INDOMETHACIN	indomethacin	CAPSULE, EXTENDED RELEASE;ORAL	202711	ANDA	Zydus Pharmaceuticals USA Inc.	68382-371	68382-371-05	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-371-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE, EXTENDED RELEASE;ORAL			Strength	75MG
Approval Date:	Sep 25, 2017	TE:	AB	RLD:	No

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