Package 69842-956-31

Brand: acetaminophen pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 69842-956-31
Digits Only 6984295631
Product NDC 69842-956
Product ID 69842-956_d8aeb795-060c-4baf-b875-1511ca7f2c0d
Description

80 TABLET, COATED in 1 BOTTLE, PLASTIC (69842-956-31)

Marketing

Marketing Status
Marketed Since 2007-12-17
Brand acetaminophen pm extra strength
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Acetaminophen PM Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8aeb795-060c-4baf-b875-1511ca7f2c0d", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["67a190c3-7de0-4f57-be94-d6b8285e1220"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, COATED in 1 BOTTLE, PLASTIC (69842-956-31)", "package_ndc": "69842-956-31", "marketing_start_date": "20071217"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "69842-956_d8aeb795-060c-4baf-b875-1511ca7f2c0d", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69842-956", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen 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": "20071217", "listing_expiration_date": "20261231"}