Search by Drug Name or NDC

NDC 43063-0671-30 Etodolac 500 mg/1 Details

Etodolac 500 mg/1

Etodolac is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx 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: 43063-0671-30
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Etodolac

Product Information

NDC	43063-0671
Product ID	43063-671_f98acaf6-d181-3c0c-e053-6394a90a62fe
Associated GPIs	66100008000320
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	500
Active Ingredient Units	mg/1
Substance Name	ETODOLAC
Labeler Name	PD-Rx 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	ANDA076004
Listing Certified Through	2024-12-31

Package

NDC 43063-0671-30 (43063067130)

Pricing Information	N/A
NDC Package Code	43063-671-30
Billing NDC	43063067130
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-671-30)
Marketing Start Date	2018-01-16
NDC Exclude Flag	N