NDC 58602-832

Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Headache

Naproxen Sodium And Pseudoephedrine Hydrochloride

Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Headache is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Aurohealth Llc. The primary component is Naproxen Sodium; Pseudoephedrine Hydrochloride.

Product ID58602-832_10a8a74b-11d1-490e-87e7-d705fe0e7602
NDC58602-832
Product TypeHuman Otc Drug
Proprietary NameNaproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Headache
Generic NameNaproxen Sodium And Pseudoephedrine Hydrochloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2022-06-01
Marketing CategoryANDA /
Application NumberANDA211360
Labeler NameAurohealth LLC
Substance NameNAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength220 mg/1; mg/1
Pharm ClassesAdrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 58602-832-67

2 BLISTER PACK in 1 CARTON (58602-832-67) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2022-06-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and Headache" or generic name "Naproxen Sodium And Pseudoephedrine Hydrochloride"

NDCBrand NameGeneric Name
58602-832Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and HeadacheNaproxen Sodium and Pseudoephedrine Hydrochloride
58602-816Naproxen Sodium and Pseudoephedrine Hydrochloride Sinus and ColdNaproxen Sodium and Pseudoephedrine Hydrochloride
50580-539SudafedNaproxen sodium and Pseudoephedrine Hydrochloride
50580-434Sudafed Sinus 12 Hour Pressure plus PainNaproxen sodium and Pseudoephedrine Hydrochloride

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