Package 0135-0539-02

Brand: panadol

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0135-0539-02
Digits Only 0135053902
Product NDC 0135-0539
Description

1 BOTTLE in 1 CARTON (0135-0539-02) / 54.7 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2012-10-15
Brand panadol
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10c14ee5-017b-0434-e063-6394a90af0f4", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["95801755-db54-4ad7-bec1-52671914f6ca"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0539-02)  / 54.7 mL in 1 BOTTLE", "package_ndc": "0135-0539-02", "marketing_start_date": "20121015"}], "brand_name": "PANADOL", "product_id": "0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4", "dosage_form": "SUSPENSION", "product_ndc": "0135-0539", "generic_name": "acetaminophen", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20121015", "listing_expiration_date": "20261231"}