Package 0135-7031-01

Brand: panadol cold and flu nondrowsy

Generic: acetaminophen and phenyleprine hcl
NDC Package

Package Facts

Identity

Package NDC 0135-7031-01
Digits Only 0135703101
Product NDC 0135-7031
Description

50 PACKET in 1 CARTON (0135-7031-01) / 2 TABLET, FILM COATED in 1 PACKET

Marketing

Marketing Status
Marketed Since 2022-12-20
Brand panadol cold and flu nondrowsy
Generic acetaminophen and phenyleprine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cbe5e2d-4776-3d99-e063-6294a90a10a9", "openfda": {"unii": ["362O9ITL9D", "04JA59TNSJ"], "rxcui": ["1046378"], "spl_set_id": ["fa0ce51f-441d-4409-8617-b3402b00f187"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 CARTON (0135-7031-01)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "0135-7031-01", "marketing_start_date": "20221220"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BLISTER PACK (0135-7031-02)", "package_ndc": "0135-7031-02", "marketing_start_date": "20221220"}], "brand_name": "Panadol Cold and Flu NonDrowsy", "product_id": "0135-7031_1cbe5e2d-4776-3d99-e063-6294a90a10a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0135-7031", "generic_name": "acetaminophen and phenyleprine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Panadol", "brand_name_suffix": "Cold and Flu NonDrowsy", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221220", "listing_expiration_date": "20261231"}