Package 72162-1078-1

Brand: pilocarpine hydrochloride

Generic: pilocarpine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1078-1
Digits Only 7216210781
Product NDC 72162-1078
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-1078-1)

Marketing

Marketing Status
Marketed Since 2024-12-12
Brand pilocarpine hydrochloride
Generic pilocarpine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aa0c11f4-3998-4089-80b7-b6807c77ecd3", "openfda": {"unii": ["0WW6D218XJ"], "rxcui": ["1000913"], "spl_set_id": ["06c054af-62b4-4373-813a-9bb2e5c92316"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1078-1)", "package_ndc": "72162-1078-1", "marketing_start_date": "20241212"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "72162-1078_aa0c11f4-3998-4089-80b7-b6807c77ecd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "72162-1078", "generic_name": "Pilocarpine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077220", "marketing_category": "ANDA", "marketing_start_date": "20051014", "listing_expiration_date": "20261231"}