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NDC 70518-3023-03 meloxicam 7.5 mg/1 Details

meloxicam 7.5 mg/1

meloxicam is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is MELOXICAM.

MedlinePlus Drug Summary

Meloxicam is 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). Meloxicam is also used to relieve the pain, tenderness, swelling, and stiffness caused by juvenile rheumatoid arthritis (a type of arthritis that affects children) in children 2 years of age and older. Meloxicam is in a class of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). It works by stopping the body's production of a substance that causes pain, fever, and inflammation.

Related Packages: 70518-3023-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Meloxicam

Product Information

NDC	70518-3023
Product ID	70518-3023_fd119534-c858-28d8-e053-6294a90ad419
Associated GPIs
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	meloxicam
Proprietary Name Suffix	n/a
Non-Proprietary Name	meloxicam
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	7.5
Active Ingredient Units	mg/1
Substance Name	MELOXICAM
Labeler Name	REMEDYREPACK 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	ANDA077921
Listing Certified Through	2024-12-31

Package

NDC 70518-3023-03 (70518302303)

Pricing Information	N/A
NDC Package Code	70518-3023-3
Billing NDC	70518302303
Package	90 TABLET in 1 BOTTLE, PLASTIC (70518-3023-3)
Marketing Start Date	2022-09-07
NDC Exclude Flag	N