Package 37808-795-03

Brand: pain relief pm extra strength

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 37808-795-03
Digits Only 3780879503
Product NDC 37808-795
Product ID 37808-795_458b73eb-31e7-5cf1-e063-6294a90a5c79
Description

1 BOTTLE, PLASTIC in 1 CARTON (37808-795-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2013-02-01
Brand pain relief pm extra strength
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Pain Relief PM Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "458b73eb-31e7-5cf1-e063-6294a90a5c79", "openfda": {"upc": ["0041220280902"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["f7958347-4e9c-4698-8749-7ca7023ee2ba"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-795-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-795-03", "marketing_start_date": "20130201"}], "brand_name": "Pain Relief PM Extra Strength", "product_id": "37808-795_458b73eb-31e7-5cf1-e063-6294a90a5c79", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-795", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "brand_name_suffix": "Extra Strength", "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": "20130201", "listing_expiration_date": "20261231"}