Package 55910-655-10

Brand: pain relief pm extra strength

Generic: acetaminophen and diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 55910-655-10
Digits Only 5591065510
Product NDC 55910-655
Description

1 BOTTLE, PLASTIC in 1 CARTON (55910-655-10) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2007-12-17
Brand pain relief pm extra strength
Generic acetaminophen and diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2954583f-051a-46a2-92f5-9051571ef123", "openfda": {"upc": ["0350844556318"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["8e65478b-7a7b-416c-b8e3-23dad79f8cc1"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (55910-655-10)  / 40 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "55910-655-10", "marketing_start_date": "20071217"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (55910-655-31)  / 80 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "55910-655-31", "marketing_start_date": "20071217"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "55910-655_2954583f-051a-46a2-92f5-9051571ef123", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-655", "generic_name": "Acetaminophen and Diphenhydramine HCl", "labeler_name": "DOLGENCORP, 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": "20071217", "listing_expiration_date": "20261231"}