NDC 71335-1282 – Naproxen

Naproxen Sodium 220 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71335-1282

Product details

Brand name
Naproxen
Generic name
Naproxen Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204872
Marketed since
January 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Naproxen →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1282-120 TABLET in 1 BOTTLE (71335-1282-1)Nov 18, 2021
71335-1282-230 TABLET in 1 BOTTLE (71335-1282-2)Aug 27, 2019
71335-1282-340 TABLET in 1 BOTTLE (71335-1282-3)Oct 22, 2019
71335-1282-450 TABLET in 1 BOTTLE (71335-1282-4)Jan 10, 2025
71335-1282-560 TABLET in 1 BOTTLE (71335-1282-5)Jan 30, 2025
71335-1282-614 TABLET in 1 BOTTLE (71335-1282-6)Nov 26, 2019
71335-1282-7100 TABLET in 1 BOTTLE (71335-1282-7)Oct 25, 2019
71335-1282-890 TABLET in 1 BOTTLE (71335-1282-8)Jan 30, 2025
71335-1282-924 TABLET in 1 BOTTLE (71335-1282-9)Jan 30, 2025

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