Package 0280-1580-20

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

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0280-1580-20
Digits Only 0280158020
Product NDC 0280-1580
Product ID 0280-1580_45267a4c-d228-b1b5-e063-6394a90a81bf
Description

1 KIT in 1 CARTON (0280-1580-20) * 2 BLISTER PACK in 1 CARTON / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-05-22
Brand alka-seltzer plus maximum strength day and night cold and flu
Generic acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45267a4c-d228-b1b5-e063-6394a90a81bf", "openfda": {"upc": ["0016500555315"], "rxcui": ["1086997", "1297288", "2634363"], "spl_set_id": ["51c44970-06e5-082e-e054-00144ff88e88"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-1580-20)  *  2 BLISTER PACK in 1 CARTON / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  2 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-1580-20", "marketing_start_date": "20170522"}], "brand_name": "Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu", "product_id": "0280-1580_45267a4c-d228-b1b5-e063-6394a90a81bf", "dosage_form": "KIT", "product_ndc": "0280-1580", "generic_name": "Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170522", "listing_expiration_date": "20261231"}