Package 51013-668-01

Brand: ultra concentrated nighttime cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
NDC Package

Package Facts

Identity

Package NDC 51013-668-01
Digits Only 5101366801
Product NDC 51013-668
Description

1 BLISTER PACK in 1 CARTON (51013-668-01) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-03-12
Brand ultra concentrated nighttime cold and flu
Generic acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "300bf27f-7450-7366-e063-6394a90acbcb", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1426334"], "spl_set_id": ["300bf27f-744f-7366-e063-6394a90acbcb"], "manufacturer_name": ["PuraCap Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51013-668-01)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "51013-668-01", "marketing_start_date": "20250312"}], "brand_name": "Ultra Concentrated Nighttime COLD AND FLU", "product_id": "51013-668_300bf27f-7450-7366-e063-6394a90acbcb", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "51013-668", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate", "labeler_name": "PuraCap Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Concentrated Nighttime COLD AND FLU", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250312", "listing_expiration_date": "20261231"}