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NDC 00185-0687-10 Etodolac 500 mg/1 Details

Etodolac 500 mg/1

Etodolac is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eon Labs, Inc.. The primary component is ETODOLAC.

MedlinePlus Drug Summary

Etodolac tablets, capsules, and extended-release (long-acting) tablets are used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Etodolac tablets and capsules are also used to relieve pain from other causes. Etodolac is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 00185-0687-10
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Etodolac

Product Information

NDC	00185-0687
Product ID	0185-0687_dae8e40e-6203-45b5-8273-61594af39245
Associated GPIs	66100008000320
GCN Sequence Number	027368
GCN Sequence Number Description	etodolac TABLET 500 MG ORAL
HIC3	S2B
HIC3 Description	NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
GCN	61766
HICL Sequence Number	006089
HICL Sequence Number Description	ETODOLAC
Brand/Generic	Generic
Proprietary Name	Etodolac
Proprietary Name Suffix	n/a
Non-Proprietary Name	Etodolac
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, COATED
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	ETODOLAC
Labeler Name	Eon Labs, Inc.
Pharmaceutical Class	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA074903
Listing Certified Through	n/a

Package

NDC 00185-0687-10 (00185068710)

Pricing Information	N/A
NDC Package Code	0185-0687-10
Billing NDC	00185068710
Package	1000 TABLET, COATED in 1 BOTTLE (0185-0687-10)
Marketing Start Date	2015-04-20
NDC Exclude Flag	N