Package 49035-531-12

Brand: acetaminophen extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 49035-531-12
Digits Only 4903553112
Product NDC 49035-531
Product ID 49035-531_fc13cf5e-0421-4c83-a132-e33d883d28cb
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49035-531-12)

Marketing

Marketing Status
Marketed Since 2005-12-11
Brand acetaminophen extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc13cf5e-0421-4c83-a132-e33d883d28cb", "openfda": {"upc": ["0681131235204"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["aa714a01-fb56-463c-9fab-257fa4996559"], "manufacturer_name": ["Wal-Mart Stores Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49035-531-12)", "package_ndc": "49035-531-12", "marketing_start_date": "20051211"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "49035-531_fc13cf5e-0421-4c83-a132-e33d883d28cb", "dosage_form": "TABLET, FILM COATED", "product_ndc": "49035-531", "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": "20051211", "listing_expiration_date": "20261231"}