Package 49580-0501-8

Brand: severe cold and cough relief daytime

Generic: acetaminohpen, dextromethorphan hbr, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 49580-0501-8
Digits Only 4958005018
Product NDC 49580-0501
Product ID 49580-0501_a105492f-6843-463d-8a44-01d89916d833
Description

245 mL in 1 BOTTLE, PLASTIC (49580-0501-8)

Marketing

Marketing Status
Marketed Since 2021-03-26
Brand severe cold and cough relief daytime
Generic acetaminohpen, dextromethorphan hbr, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Severe Cold and Cough Relief Daytime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a105492f-6843-463d-8a44-01d89916d833", "openfda": {"upc": ["0349580501836"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1113705"], "spl_set_id": ["2af496a1-6fdd-4acf-9944-8b7cdf302275"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245 mL in 1 BOTTLE, PLASTIC (49580-0501-8)", "package_ndc": "49580-0501-8", "marketing_start_date": "20210326"}], "brand_name": "Severe Cold and Cough Relief Daytime", "product_id": "49580-0501_a105492f-6843-463d-8a44-01d89916d833", "dosage_form": "LIQUID", "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": "49580-0501", "generic_name": "ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Cold and Cough Relief", "brand_name_suffix": "Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210326", "listing_expiration_date": "20261231"}