Package 11822-4530-2

Brand: sinus pressure and congestion relief pe maximum strength

Generic: phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 11822-4530-2
Digits Only 1182245302
Product NDC 11822-4530
Description

3 BLISTER PACK in 1 CARTON (11822-4530-2) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2005-01-14
Brand sinus pressure and congestion relief pe maximum strength
Generic phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c0b091a6-20f7-42cb-a1de-3e1dfba0611e", "openfda": {"upc": ["0011822041751"], "unii": ["04JA59TNSJ"], "rxcui": ["1049182"], "spl_set_id": ["fccea3c5-42af-4939-82bc-d9409b75f91f"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (11822-4530-2)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11822-4530-2", "marketing_start_date": "20050114"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11822-4530-4)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11822-4530-4", "marketing_start_date": "20050114"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11822-4530-7)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11822-4530-7", "marketing_start_date": "20050114"}], "brand_name": "Sinus Pressure and Congestion Relief PE Maximum Strength", "product_id": "11822-4530_c0b091a6-20f7-42cb-a1de-3e1dfba0611e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "11822-4530", "generic_name": "Phenylephrine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Pressure and Congestion Relief PE", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050114", "listing_expiration_date": "20261231"}