Package 63941-095-02
Brand: extra strength pain relief pm
Generic: acetaminophen and diphenhydramine hydrochloridePackage 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
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"}