NDC 69230-329 – Naproxen sodium

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

Human Otc Drug

Product NDC69230-329

Product details

Brand name
Naproxen sodium
Generic name
Naproxen sodium
Labeler
Camber Consumer Care Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211065
Marketed since
October 28, 2022
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 (6)

Package NDCDescriptionSince
69230-329-011 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLEOct 28, 2022
69230-329-021 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLEOct 28, 2022
69230-329-05500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)Oct 28, 2022
69230-329-101000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10)Oct 28, 2022
69230-329-241 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLEOct 28, 2022
69230-329-501 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLEOct 28, 2022

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