Package 60219-5922-1

Brand: pilocarpine hydrochloride

Generic: pilocarpine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60219-5922-1
Digits Only 6021959221
Product NDC 60219-5922
Description

100 TABLET, FILM COATED in 1 BOTTLE (60219-5922-1)

Marketing

Marketing Status
Marketed Since 2007-05-01
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": "fceac8ec-dd40-4a49-bdb4-5b02a759a4a3", "openfda": {"upc": ["0360219592216"], "unii": ["0WW6D218XJ"], "rxcui": ["1000913"], "spl_set_id": ["6272ccac-b543-404d-9938-8583bb59ed2c"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60219-5922-1)", "package_ndc": "60219-5922-1", "marketing_start_date": "20070501"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "60219-5922_fceac8ec-dd40-4a49-bdb4-5b02a759a4a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "60219-5922", "generic_name": "PILOCARPINE HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077248", "marketing_category": "ANDA", "marketing_start_date": "20070501", "listing_expiration_date": "20261231"}