Package 0280-1590-20

Brand: alka-seltzer plus maximum strength day cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0280-1590-20
Digits Only 0280159020
Product NDC 0280-1590
Description

2 BLISTER PACK in 1 CARTON (0280-1590-20) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-06-19
Brand alka-seltzer plus maximum strength day cold and flu
Generic acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45267943-6d50-45dd-e063-6294a90ab025", "openfda": {"upc": ["0016500555308"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["5172dc01-4e7f-3307-e054-00144ff8d46c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-1590-20)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-1590-20", "marketing_start_date": "20170619"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Day Cold and Flu", "product_id": "0280-1590_45267943-6d50-45dd-e063-6294a90ab025", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0280-1590", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Day Cold and Flu", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170619", "listing_expiration_date": "20261231"}