NDC 50844-604 – Naproxen Sodium

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

Human Otc Drug

Product NDC50844-604

Product details

Brand name
Naproxen Sodium
Generic name
Naproxen Sodium
Labeler
L.N.K. International, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204872
Marketed since
February 1, 2017
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
50844-604-06200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06)Feb 19, 2026
50844-604-094 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACKFeb 1, 2017
50844-604-14500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-14)Feb 1, 2017
50844-604-151 BOTTLE, PLASTIC in 1 CARTON (50844-604-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTICFeb 1, 2017
50844-604-161000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-16)Feb 1, 2017
50844-604-191 BOTTLE, PLASTIC in 1 CARTON (50844-604-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTICFeb 1, 2017
50844-604-5625 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-56)Feb 1, 2017
50844-604-988 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-98)Feb 1, 2017
50844-604-998 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-99)Feb 1, 2017

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