Package 76168-119-25

Brand: pain relief pm

Generic: acetaminophen pm
NDC Package

Package Facts

Identity

Package NDC 76168-119-25
Digits Only 7616811925
Product NDC 76168-119
Description

50 CARTON in 1 BOTTLE (76168-119-25) / 1 TABLET in 1 CARTON

Marketing

Marketing Status
Marketed Since 2018-05-14
Brand pain relief pm
Generic acetaminophen pm
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c30260f-b9e7-58c3-e053-2991aa0a818c", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["c1c1de91-6a54-4d91-93a9-b6be6d7c7dfb"], "manufacturer_name": ["Velocity Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTON in 1 BOTTLE (76168-119-25)  / 1 TABLET in 1 CARTON", "package_ndc": "76168-119-25", "marketing_start_date": "20180514"}], "brand_name": "Pain Relief PM", "product_id": "76168-119_6c30260f-b9e7-58c3-e053-2991aa0a818c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "76168-119", "generic_name": "Acetaminophen PM", "labeler_name": "Velocity Pharma", "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": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20121205", "listing_expiration_date": "20261231"}