Package 0280-0152-02

Brand: alka-seltzer plus cough and sore throat fizzychews

Generic: acetaminophen, dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 0280-0152-02
Digits Only 0280015202
Product NDC 0280-0152
Description

3 BLISTER PACK in 1 CARTON (0280-0152-02) / 8 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-04-01
Brand alka-seltzer plus cough and sore throat fizzychews
Generic acetaminophen, dextromethorphan hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "452660a4-50ec-ef65-e063-6294a90ad533", "openfda": {"upc": ["0016500601715"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2678223"], "spl_set_id": ["14951faa-9476-6f29-e063-6394a90a14c7"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0152-01)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0280-0152-01", "marketing_start_date": "20240401"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0280-0152-02)  / 8 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0280-0152-02", "marketing_start_date": "20240401"}], "brand_name": "Alka-Seltzer Plus Cough and Sore Throat FizzyChews", "product_id": "0280-0152_452660a4-50ec-ef65-e063-6294a90ad533", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0280-0152", "generic_name": "acetaminophen, dextromethorphan hydrobromide", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Cough and Sore Throat FizzyChews", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "162.5 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}