Package 84324-005-01

Brand: pain relief pm

Generic: acetaminophen, diphenhydramine
NDC Package

Package Facts

Identity

Package NDC 84324-005-01
Digits Only 8432400501
Product NDC 84324-005
Product ID 84324-005_e2670c20-2955-459d-b011-cdc0a6d93893
Description

100 TABLET in 1 BOTTLE (84324-005-01)

Marketing

Marketing Status
Marketed Since 2024-07-30
Brand pain relief pm
Generic acetaminophen, diphenhydramine
Sample Package No

Linked Drug Pages (1)

Pain Relief PM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e2670c20-2955-459d-b011-cdc0a6d93893", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["32a5611b-9bf6-4850-a7ff-fa240da04f45"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (84324-005-01)", "package_ndc": "84324-005-01", "marketing_start_date": "20240730"}], "brand_name": "Pain Relief PM", "product_id": "84324-005_e2670c20-2955-459d-b011-cdc0a6d93893", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "84324-005", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE", "labeler_name": "NUVICARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief 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": "20240730", "listing_expiration_date": "20261231"}