Package 70264-028-01

Brand: tylenol pm extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70264-028-01
Digits Only 7026402801
Product NDC 70264-028
Product ID 70264-028_43c8c37c-62db-f6e0-e063-6394a90aab46
Description

50 POUCH in 1 BOX (70264-028-01) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2021-05-01
Brand tylenol pm extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

TYLENOL PM EXTRA STRENGTH ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c8c37c-62db-f6e0-e063-6394a90aab46", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["a40ea0e3-d666-4605-b5e0-beeaf8f586f2"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (70264-028-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "70264-028-01", "marketing_start_date": "20210501"}], "brand_name": "TYLENOL PM EXTRA STRENGTH", "product_id": "70264-028_43c8c37c-62db-f6e0-e063-6394a90aab46", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70264-028", "generic_name": "ACETAMINOPHEN", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL PM 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": "20210501", "listing_expiration_date": "20261231"}