NDC 71335-2080 – Meloxicam

Meloxicam 7.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2080

Product details

Brand name
Meloxicam
Generic name
Meloxicam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077921
Marketed since
July 19, 2006
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
71335-2080-0120 TABLET in 1 BOTTLE (71335-2080-0)Oct 31, 2024
71335-2080-130 TABLET in 1 BOTTLE (71335-2080-1)Jul 6, 2022
71335-2080-260 TABLET in 1 BOTTLE (71335-2080-2)Jun 3, 2022
71335-2080-3100 TABLET in 1 BOTTLE (71335-2080-3)Oct 31, 2024
71335-2080-490 TABLET in 1 BOTTLE (71335-2080-4)May 9, 2022
71335-2080-514 TABLET in 1 BOTTLE (71335-2080-5)Sep 9, 2022
71335-2080-610 TABLET in 1 BOTTLE (71335-2080-6)Oct 31, 2024
71335-2080-756 TABLET in 1 BOTTLE (71335-2080-7)Oct 31, 2024
71335-2080-828 TABLET in 1 BOTTLE (71335-2080-8)Aug 22, 2022
71335-2080-920 TABLET in 1 BOTTLE (71335-2080-9)Oct 31, 2024

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