Package 0135-0609-04
Brand: panadol extra strength
Generic: acetaminophenPackage Facts
Identity
Package NDC
0135-0609-04
Digits Only
0135060904
Product NDC
0135-0609
Description
50 PACKET in 1 CARTON (0135-0609-04) / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)
Marketing
Marketing Status
Brand
panadol 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": "10c10ae1-2b66-f708-e063-6394a90a0fca", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "200977"], "spl_set_id": ["b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-01) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-01", "marketing_start_date": "20170315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-02) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-02", "marketing_start_date": "20170315"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0609-03) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0135-0609-03", "marketing_start_date": "20170315"}, {"sample": false, "description": "50 PACKET in 1 CARTON (0135-0609-04) / 2 TABLET, FILM COATED in 1 PACKET (0135-0609-05)", "package_ndc": "0135-0609-04", "marketing_start_date": "20170315"}], "brand_name": "PANADOL Extra Strength", "product_id": "0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0135-0609", "generic_name": "acetaminophen", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170315", "listing_expiration_date": "20261231"}