Package 68071-2356-1

Brand: DOXEPIN HYDROCHLORIDE

Generic: DOXEPIN HYDROCHLORIDE
NDC Package

Package Facts

Identity

Package NDC 68071-2356-1
Digits Only 6807123561
Product NDC 68071-2356
Product ID 68071-2356_2b5c46fa-bfd7-c890-e063-6294a90a8759
Description

100 CAPSULE in 1 BOTTLE (68071-2356-1)

Marketing

Marketing Status
Marketed Since 2021-03-08
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": "2b5c46fa-bfd7-c890-e063-6294a90a8759", "openfda": {"upc": ["0368071235616"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["bd0a04e2-cd1d-bd3f-e053-2995a90a7c81"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-2356-1)", "package_ndc": "68071-2356-1", "marketing_start_date": "20210308"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "68071-2356_2b5c46fa-bfd7-c890-e063-6294a90a8759", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-2356", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213063", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}