Package 63941-095-02

Brand: extra strength pain relief pm

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63941-095-02
Digits Only 6394109502
Product NDC 63941-095
Description

1 BOTTLE, PLASTIC in 1 CARTON (63941-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-10-31
Brand extra strength pain relief 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": "45b0d446-7d54-c0c8-e063-6294a90a5230", "openfda": {"upc": ["0070038201786"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["f8820150-feec-4062-85bb-14525ddf691f"], "manufacturer_name": ["VALU MERCHANDISERS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-095-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-02", "marketing_end_date": "20271031", "marketing_start_date": "20100201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63941-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-03", "marketing_end_date": "20271231", "marketing_start_date": "20111004"}, {"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (63941-095-09)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63941-095-09", "marketing_end_date": "20280331", "marketing_start_date": "20120203"}], "brand_name": "Extra Strength Pain Relief PM", "product_id": "63941-095_45b0d446-7d54-c0c8-e063-6294a90a5230", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63941-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "VALU MERCHANDISERS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength 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_end_date": "20280331", "marketing_start_date": "20100201"}