NDC 71335-0406 – Meloxicam

Meloxicam 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0406

Product details

Brand name
Meloxicam
Generic name
Meloxicam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077927
Marketed since
March 7, 2007
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Meloxicam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0406-0120 TABLET in 1 BOTTLE (71335-0406-0)Mar 28, 2018
71335-0406-130 TABLET in 1 BOTTLE (71335-0406-1)Apr 9, 2018
71335-0406-260 TABLET in 1 BOTTLE (71335-0406-2)Mar 27, 2018
71335-0406-3100 TABLET in 1 BOTTLE (71335-0406-3)Nov 11, 2021
71335-0406-490 TABLET in 1 BOTTLE (71335-0406-4)Mar 7, 2018
71335-0406-514 TABLET in 1 BOTTLE (71335-0406-5)May 9, 2018
71335-0406-610 TABLET in 1 BOTTLE (71335-0406-6)Apr 1, 2019
71335-0406-756 TABLET in 1 BOTTLE (71335-0406-7)Feb 15, 2018
71335-0406-828 TABLET in 1 BOTTLE (71335-0406-8)Jul 24, 2019
71335-0406-920 TABLET in 1 BOTTLE (71335-0406-9)Mar 9, 2022

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