Package 72189-161-30

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-161-30
Digits Only 7218916130
Product NDC 72189-161
Product ID 72189-161_2be91ea1-1f2a-d635-e063-6294a90a4dd1
Description

30 CAPSULE in 1 BOTTLE (72189-161-30)

Marketing

Marketing Status
Marketed Since 2020-12-01
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

DOXEPIN HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be91ea1-1f2a-d635-e063-6294a90a4dd1", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000070"], "spl_set_id": ["b56cdaee-6187-c763-e053-2995a90acc3f"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-161-30)", "package_ndc": "72189-161-30", "marketing_start_date": "20201201"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "72189-161_2be91ea1-1f2a-d635-e063-6294a90a4dd1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-161", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213063", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}