Package 71335-2601-3
Brand: imipramine hydrochloride
Generic: imipramine hydrochloridePackage Facts
Identity
Package NDC
71335-2601-3
Digits Only
7133526013
Product NDC
71335-2601
Description
90 TABLET, FILM COATED in 1 BOTTLE (71335-2601-3)
Marketing
Marketing Status
Brand
imipramine hydrochloride
Generic
imipramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47b2a18c-4497-42e0-a2fe-8e8f2761400e", "openfda": {"unii": ["BKE5Q1J60U"], "rxcui": ["835564"], "spl_set_id": ["20af582f-08ba-4281-a2df-0bcf68c58594"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2601-1)", "package_ndc": "71335-2601-1", "marketing_start_date": "20250605"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2601-2)", "package_ndc": "71335-2601-2", "marketing_start_date": "20250605"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2601-3)", "package_ndc": "71335-2601-3", "marketing_start_date": "20250605"}], "brand_name": "Imipramine Hydrochloride", "product_id": "71335-2601_47b2a18c-4497-42e0-a2fe-8e8f2761400e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-2601", "generic_name": "Imipramine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040903", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}