Package 36800-095-03

Brand: pain relief pm extra strength

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 36800-095-03
Digits Only 3680009503
Product NDC 36800-095
Description

1 BOTTLE, PLASTIC in 1 CARTON (36800-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2012-11-30
Brand pain relief pm extra strength
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ff37f0e-3a25-dfd8-e063-6394a90ae3ca", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["3b672ec7-8658-4b43-a79d-094ac8bc6904"], "manufacturer_name": ["TopCo Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "36800-095-03", "marketing_start_date": "20121130"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (36800-095-17)", "package_ndc": "36800-095-17", "marketing_start_date": "20190321"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "36800-095_3ff37f0e-3a25-dfd8-e063-6394a90ae3ca", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "36800-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "TopCo Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20121130", "listing_expiration_date": "20261231"}