Package 0363-8995-24

Brand: severe cold and flu daytime non drowsy and nighttime

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

Package Facts

Identity

Package NDC 0363-8995-24
Digits Only 0363899524
Product NDC 0363-8995
Description

1 KIT in 1 PACKAGE, COMBINATION (0363-8995-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-06-30
Brand severe cold and flu daytime non drowsy and nighttime
Generic acetaminophen, dextromethorphan hydrobromide,guaifenesin, phenylephrine hydrochloride / acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "48c1f99d-1e71-df3c-e063-6294a90a346c", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["2dba2bec-e0e3-4910-89c5-ebc093e05bec"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0363-8995-24)  *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0363-8995-24", "marketing_end_date": "20270630", "marketing_start_date": "20210823"}], "brand_name": "SEVERE COLD AND FLU DAYTIME NON DROWSY and NIGHTTIME", "product_id": "0363-8995_48c1f99d-1e71-df3c-e063-6294a90a346c", "dosage_form": "KIT", "product_ndc": "0363-8995", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE / ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SEVERE COLD AND FLU", "brand_name_suffix": "DAYTIME NON DROWSY and NIGHTTIME", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270630", "marketing_start_date": "20210823"}