NDC 58602-816 – Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Cold

Naproxen Sodium 220 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC58602-816

Product details

Brand name
Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Cold
Generic name
Naproxen Sodium and Pseudoephedrine Hydrochloride
Labeler
Aurohealth LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211360
Marketed since
June 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug; alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Cold →

Package NDC codes (3)

Package NDCDescriptionSince
58602-816-672 BLISTER PACK in 1 CARTON (58602-816-67) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 1, 2022
58602-816-723 BLISTER PACK in 1 CARTON (58602-816-72) / 8 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 12, 2025
58602-816-831 BLISTER PACK in 1 CARTON (58602-816-83) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 1, 2022