Package 49035-175-15

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49035-175-15
Digits Only 4903517515
Product NDC 49035-175
Description

1 BOTTLE, PLASTIC in 1 CARTON (49035-175-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 1993-04-02
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bbab41dd-70e6-4f83-a5cb-262e683a77ae", "openfda": {"upc": ["0681131133548"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["78874258-16cc-40b5-9e15-5943eddfce94"], "manufacturer_name": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (49035-175-15)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "49035-175-15", "marketing_start_date": "19930402"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "49035-175_bbab41dd-70e6-4f83-a5cb-262e683a77ae", "dosage_form": "TABLET, FILM COATED", "product_ndc": "49035-175", "generic_name": "Acetaminophen", "labeler_name": "Wal-Mart Stores Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19930402", "listing_expiration_date": "20261231"}