Package 63029-053-90

Brand: percogesic original strength

Generic: acetaminophen and diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 63029-053-90
Digits Only 6302905390
Product NDC 63029-053
Description

1 BOTTLE, PLASTIC in 1 BOX (63029-053-90) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2010-03-19
Brand percogesic original strength
Generic acetaminophen and diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6a927a49-32fc-4139-b0fe-7d2520495273", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1052462", "1052466"], "spl_set_id": ["529974c2-0121-4892-8e47-c2c447581091"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (63029-053-90)  / 90 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63029-053-90", "marketing_start_date": "20100319"}], "brand_name": "Percogesic Original Strength", "product_id": "63029-053_6a927a49-32fc-4139-b0fe-7d2520495273", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63029-053", "generic_name": "Acetaminophen and Diphenhydramine HCl", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Percogesic", "brand_name_suffix": "Original Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100319", "listing_expiration_date": "20261231"}