Package 49035-363-24

Brand: pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 49035-363-24
Digits Only 4903536324
Product NDC 49035-363
Description

1 BOTTLE, PLASTIC in 1 BOX (49035-363-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2020-01-31
Brand pain reliever pm extra strength
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "deb6f37e-6918-4276-81c2-638b9dd51cfe", "openfda": {"upc": ["0681131357302"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["79886972-47a4-44c5-a131-1a691a328103"], "manufacturer_name": ["EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (49035-363-10)", "package_ndc": "49035-363-10", "marketing_start_date": "20200131"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49035-363-24)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "49035-363-24", "marketing_start_date": "20200131"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (49035-363-25)", "package_ndc": "49035-363-25", "marketing_start_date": "20200131"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "49035-363_deb6f37e-6918-4276-81c2-638b9dd51cfe", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "49035-363", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever 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": "20200131", "listing_expiration_date": "20261231"}