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NDC 68788-7315-01 Etodolac 400 mg/1 Details

Etodolac 400 mg/1

Etodolac is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals 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: 68788-7315-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Etodolac

Product Information

NDC	68788-7315
Product ID	68788-7315_3434dd84-f91b-42a2-b28e-224dfdb2ed4f
Associated GPIs	66100008000310
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Etodolac
Proprietary Name Suffix	n/a
Non-Proprietary Name	Etodolac
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	400
Active Ingredient Units	mg/1
Substance Name	ETODOLAC
Labeler Name	Preferred Pharmaceuticals 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	ANDA208834
Listing Certified Through	2025-12-31

Package

NDC 68788-7315-01 (68788731501)

Pricing Information	N/A
NDC Package Code	68788-7315-1
Billing NDC	68788731501
Package	100 TABLET, FILM COATED in 1 BOTTLE (68788-7315-1)
Marketing Start Date	2019-01-02
NDC Exclude Flag	N