Package 71335-2472-2

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2472-2
Digits Only 7133524722
Product NDC 71335-2472
Description

30 CAPSULE in 1 BOTTLE (71335-2472-2)

Marketing

Marketing Status
Marketed Since 2024-11-13
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63f9452b-c437-482e-86e5-17f5a99b9a2d", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["19c8ad61-4e4f-4c59-b196-34a4e470459f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-2472-1)", "package_ndc": "71335-2472-1", "marketing_start_date": "20241113"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2472-2)", "package_ndc": "71335-2472-2", "marketing_start_date": "20241113"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-2472-3)", "package_ndc": "71335-2472-3", "marketing_start_date": "20241113"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71335-2472-4)", "package_ndc": "71335-2472-4", "marketing_start_date": "20241113"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "71335-2472_63f9452b-c437-482e-86e5-17f5a99b9a2d", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-2472", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}