Package 59651-224-01

Brand: pilocarpine hydrochloride

Generic: pilocarpine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-224-01
Digits Only 5965122401
Product NDC 59651-224
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-224-01)

Marketing

Marketing Status
Marketed Since 2019-08-13
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": "43f023b3-346b-4b93-95b9-ded7f37da9be", "openfda": {"unii": ["0WW6D218XJ"], "rxcui": ["1000913", "1001004"], "spl_set_id": ["438cfaa3-b5f6-4d75-ac22-b0b4e07bb118"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-224-01)", "package_ndc": "59651-224-01", "marketing_start_date": "20190813"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "59651-224_43f023b3-346b-4b93-95b9-ded7f37da9be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "59651-224", "generic_name": "pilocarpine hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA212377", "marketing_category": "ANDA", "marketing_start_date": "20190813", "listing_expiration_date": "20261231"}