NDC 71335-1650 – Naproxen sodium

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

Human Prescription Drug

Product NDC71335-1650

Product details

Brand name
Naproxen sodium
Generic name
Naproxen sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078486
Marketed since
April 26, 2016
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
71335-1650-06 TABLET, FILM COATED in 1 BOTTLE (71335-1650-0)Aug 12, 2024
71335-1650-120 TABLET, FILM COATED in 1 BOTTLE (71335-1650-1)Aug 12, 2024
71335-1650-2100 TABLET, FILM COATED in 1 BOTTLE (71335-1650-2)Aug 12, 2024
71335-1650-330 TABLET, FILM COATED in 1 BOTTLE (71335-1650-3)Jun 23, 2020
71335-1650-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1650-4)Aug 12, 2024
71335-1650-560 TABLET, FILM COATED in 1 BOTTLE (71335-1650-5)Aug 12, 2024
71335-1650-690 TABLET, FILM COATED in 1 BOTTLE (71335-1650-6)Aug 12, 2024
71335-1650-742 TABLET, FILM COATED in 1 BOTTLE (71335-1650-7)Aug 12, 2024
71335-1650-814 TABLET, FILM COATED in 1 BOTTLE (71335-1650-8)Aug 12, 2024
71335-1650-956 TABLET, FILM COATED in 1 BOTTLE (71335-1650-9)Aug 12, 2024

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