Package 42571-422-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42571-422-01
Digits Only 4257142201
Product NDC 42571-422
Product ID 42571-422_3a339de3-917e-a3d8-e063-6294a90a6889
Description

100 CAPSULE in 1 BOTTLE (42571-422-01)

Marketing

Marketing Status
Marketed Since 2024-01-01
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": "3a339de3-917e-a3d8-e063-6294a90a6889", "openfda": {"upc": ["0342571424015", "0342571423018", "0342571420017", "0342571422011", "0342571421014"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["8a3ba1fd-de34-47e4-96ca-f3086aed4b76"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42571-422-01)", "package_ndc": "42571-422-01", "marketing_start_date": "20240101"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42571-422-13)", "package_ndc": "42571-422-13", "marketing_start_date": "20240101"}], "brand_name": "Doxepin Hydrochloride", "product_id": "42571-422_3a339de3-917e-a3d8-e063-6294a90a6889", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "42571-422", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217688", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}