Package 71335-2120-1
Brand: pilocarpine hydrchloride
Generic: pilocarpine hydrchloridePackage Facts
Identity
Package NDC
71335-2120-1
Digits Only
7133521201
Product NDC
71335-2120
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2120-1)
Marketing
Marketing Status
Brand
pilocarpine hydrchloride
Generic
pilocarpine hydrchloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fda30c73-7230-bbca-e053-6294a90ae203", "openfda": {"unii": ["0WW6D218XJ"], "rxcui": ["1000913"], "spl_set_id": ["2a646f09-72e3-4795-8e69-40fb84d04a4f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2120-1)", "package_ndc": "71335-2120-1", "marketing_start_date": "20220620"}], "brand_name": "pilocarpine hydrchloride", "product_id": "71335-2120_fda30c73-7230-bbca-e053-6294a90ae203", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "71335-2120", "generic_name": "pilocarpine hydrchloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pilocarpine hydrchloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076746", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}