Package 36800-095-03
Brand: pain relief pm extra strength
Generic: acetaminophen and diphenhydramine hydrochloridePackage 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
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"}