Package 72162-2563-1

Brand: cevimeline hydrochloride

Generic: cevimeline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2563-1
Digits Only 7216225631
Product NDC 72162-2563
Product ID 72162-2563_fb360aef-a237-424f-95a0-f39d33113bd7
Description

100 CAPSULE in 1 BOTTLE (72162-2563-1)

Marketing

Marketing Status
Marketed Since 2025-11-04
Brand cevimeline hydrochloride
Generic cevimeline hydrochloride
Sample Package No

Linked Drug Pages (1)

Cevimeline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fb360aef-a237-424f-95a0-f39d33113bd7", "openfda": {"unii": ["P81Q6V85NP"], "rxcui": ["309140"], "spl_set_id": ["71ada1b0-3344-4202-9277-57f1a37402c1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2563-1)", "package_ndc": "72162-2563-1", "marketing_start_date": "20251104"}], "brand_name": "Cevimeline Hydrochloride", "product_id": "72162-2563_fb360aef-a237-424f-95a0-f39d33113bd7", "dosage_form": "CAPSULE", "pharm_class": ["Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "72162-2563", "generic_name": "Cevimeline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cevimeline Hydrochloride", "active_ingredients": [{"name": "CEVIMELINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA215056", "marketing_category": "ANDA", "marketing_start_date": "20230418", "listing_expiration_date": "20261231"}