Package 69315-160-10

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69315-160-10
Digits Only 6931516010
Product NDC 69315-160
Product ID 69315-160_5cc7cb1d-f51f-4a92-8bd2-59c037df9987
Description

1000 CAPSULE in 1 PACKAGE (69315-160-10)

Marketing

Marketing Status
Marketed Since 2021-04-15
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": "5cc7cb1d-f51f-4a92-8bd2-59c037df9987", "openfda": {"upc": ["0369315161104", "0369315159019", "0369315160107", "0369315162101", "0369315162019", "0369315160015", "0369315161012"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["e6a4cb10-1928-4abe-8797-404c9ddc37dd"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 PACKAGE (69315-160-01)", "package_ndc": "69315-160-01", "marketing_start_date": "20210415"}, {"sample": false, "description": "1000 CAPSULE in 1 PACKAGE (69315-160-10)", "package_ndc": "69315-160-10", "marketing_start_date": "20210415"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "69315-160_5cc7cb1d-f51f-4a92-8bd2-59c037df9987", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69315-160", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA211619", "marketing_category": "ANDA", "marketing_start_date": "20210415", "listing_expiration_date": "20261231"}