Package 57344-095-03
Brand: acetaminophen pm
Generic: acetaminophen and diphenhydramine hydrochloridePackage Facts
Identity
Package NDC
57344-095-03
Digits Only
5734409503
Product NDC
57344-095
Description
1 BOTTLE, PLASTIC in 1 CARTON (57344-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
acetaminophen pm
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": "284d3315-9077-e45f-e063-6394a90af0c4", "openfda": {"upc": ["0099581911003"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["409b5fcd-5880-4dda-85d8-26aeceb4f8ab"], "manufacturer_name": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-095-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-095-01", "marketing_start_date": "20170701"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-095-02", "marketing_start_date": "20121001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-095-03", "marketing_start_date": "20171101"}, {"sample": false, "description": "300 TABLET, COATED in 1 BOTTLE, PLASTIC (57344-095-12)", "package_ndc": "57344-095-12", "marketing_start_date": "20240312"}], "brand_name": "Acetaminophen PM", "product_id": "57344-095_284d3315-9077-e45f-e063-6394a90af0c4", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57344-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "AAA Pharmaceutical, 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": "20121001", "listing_expiration_date": "20261231"}