NDC 50844-417 – Naproxen Sodium

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

Human Otc Drug

Product NDC50844-417

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 (8)

Package NDCDescriptionSince
50844-417-1160 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)Feb 1, 2017
50844-417-14500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)Feb 1, 2017
50844-417-161000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)Feb 1, 2017
50844-417-191 BOTTLE, PLASTIC in 1 CARTON (50844-417-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTICFeb 1, 2017
50844-417-2248 POUCH in 1 CARTON (50844-417-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)Feb 1, 2017
50844-417-5625 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)Feb 1, 2017
50844-417-988 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)Feb 1, 2017
50844-417-998 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)Feb 1, 2017

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