Package 51013-320-54

Brand: extra strength acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 51013-320-54
Digits Only 5101332054
Product NDC 51013-320
Product ID 51013-320_1b2f1b11-905c-4c77-b609-ffae53749092
Description

15 POUCH in 1 CARTON (51013-320-54) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2017-11-09
Brand extra strength acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Extra Strength Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b2f1b11-905c-4c77-b609-ffae53749092", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["f3c57374-1408-4459-a4de-ad12c2fc6b61"], "manufacturer_name": ["PuraCap Pharmaceutical LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 POUCH in 1 CARTON (51013-320-54)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "51013-320-54", "marketing_start_date": "20171109"}], "brand_name": "Extra Strength Acetaminophen", "product_id": "51013-320_1b2f1b11-905c-4c77-b609-ffae53749092", "dosage_form": "TABLET, FILM COATED", "product_ndc": "51013-320", "generic_name": "Acetaminophen", "labeler_name": "PuraCap Pharmaceutical LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20171109", "listing_expiration_date": "20261231"}