Package 0280-1590-20
Brand: alka-seltzer plus maximum strength day cold and flu
Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloridePackage 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
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"}