Package 72090-032-01

Brand: pain relief pm

Generic: acetaminophen, diphenhydramine
NDC Package

Package Facts

Identity

Package NDC 72090-032-01
Digits Only 7209003201
Product NDC 72090-032
Product ID 72090-032_3534d9ad-25c0-42ed-89d8-bc28ca3488dd
Description

375 TABLET in 1 BOTTLE (72090-032-01)

Marketing

Marketing Status
Marketed Since 2024-08-29
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": "3534d9ad-25c0-42ed-89d8-bc28ca3488dd", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["0181af13-da32-4431-be39-c31fdfac9202"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "375 TABLET in 1 BOTTLE (72090-032-01)", "package_ndc": "72090-032-01", "marketing_start_date": "20240829"}], "brand_name": "Pain Relief PM", "product_id": "72090-032_3534d9ad-25c0-42ed-89d8-bc28ca3488dd", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72090-032", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE", "labeler_name": "Pioneer Life Sciences, 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": "20240829", "listing_expiration_date": "20261231"}