Package 81522-095-03

Brand: acetaminophen pm

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 81522-095-03
Digits Only 8152209503
Product NDC 81522-095
Product ID 81522-095_2499e0c3-bbc3-58aa-e063-6294a90a4ed5
Description

1 BOTTLE, PLASTIC in 1 CARTON (81522-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2023-05-02
Brand acetaminophen pm
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Acetaminophen PM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2499e0c3-bbc3-58aa-e063-6294a90a4ed5", "openfda": {"upc": ["0099581912055"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["f4322f34-ac19-371e-e053-2a95a90ac864"], "manufacturer_name": ["FSA STORE INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (81522-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "81522-095-03", "marketing_start_date": "20230502"}], "brand_name": "Acetaminophen PM", "product_id": "81522-095_2499e0c3-bbc3-58aa-e063-6294a90a4ed5", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "81522-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "FSA STORE INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen PM", "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": "20230502", "listing_expiration_date": "20261231"}