NDC 71335-1061 – Naproxen Sodium

Naproxen Sodium 220 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC71335-1061

Product details

Brand name
Naproxen Sodium
Generic name
Naproxen Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA074661
Marketed since
April 11, 2014
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 (8)

Package NDCDescriptionSince
71335-1061-120 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)Dec 28, 2021
71335-1061-230 TABLET, FILM COATED in 1 BOTTLE (71335-1061-2)Jan 16, 2019
71335-1061-340 TABLET, FILM COATED in 1 BOTTLE (71335-1061-3)Dec 28, 2021
71335-1061-450 TABLET, FILM COATED in 1 BOTTLE (71335-1061-4)Dec 28, 2021
71335-1061-560 TABLET, FILM COATED in 1 BOTTLE (71335-1061-5)Dec 28, 2021
71335-1061-614 TABLET, FILM COATED in 1 BOTTLE (71335-1061-6)Dec 28, 2021
71335-1061-7100 TABLET, FILM COATED in 1 BOTTLE (71335-1061-7)Dec 28, 2021
71335-1061-890 TABLET, FILM COATED in 1 BOTTLE (71335-1061-8)Dec 28, 2021

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