NDC 71335-0822 – Naproxen Sodium

Naproxen Sodium 550 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0822

Product details

Brand name
Naproxen Sodium
Generic name
Naproxen Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200629
Marketed since
October 31, 2011
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Naproxen Sodium →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0822-06 TABLET, FILM COATED in 1 BOTTLE (71335-0822-0)Jan 29, 2025
71335-0822-120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-1)Feb 21, 2020
71335-0822-2100 TABLET, FILM COATED in 1 BOTTLE (71335-0822-2)Jan 29, 2025
71335-0822-330 TABLET, FILM COATED in 1 BOTTLE (71335-0822-3)Aug 23, 2018
71335-0822-4120 TABLET, FILM COATED in 1 BOTTLE (71335-0822-4)May 29, 2018
71335-0822-560 TABLET, FILM COATED in 1 BOTTLE (71335-0822-5)Apr 26, 2018
71335-0822-690 TABLET, FILM COATED in 1 BOTTLE (71335-0822-6)Jan 29, 2025
71335-0822-742 TABLET, FILM COATED in 1 BOTTLE (71335-0822-7)Jan 29, 2025
71335-0822-814 TABLET, FILM COATED in 1 BOTTLE (71335-0822-8)Jan 29, 2025
71335-0822-956 TABLET, FILM COATED in 1 BOTTLE (71335-0822-9)Jan 29, 2025

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