Package 68071-5179-9

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5179-9
Digits Only 6807151799
Product NDC 68071-5179
Description

90 CAPSULE in 1 BOTTLE (68071-5179-9)

Marketing

Marketing Status
Marketed Since 2020-02-18
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": "1b569e5e-9af4-79a6-e063-6394a90a1647", "openfda": {"upc": ["0368071517996"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["9ee26b24-7121-3107-e053-2995a90ac61c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68071-5179-9)", "package_ndc": "68071-5179-9", "marketing_start_date": "20200218"}], "brand_name": "Doxepin Hydrochloride", "product_id": "68071-5179_1b569e5e-9af4-79a6-e063-6394a90a1647", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-5179", "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": "ANDA211603", "marketing_category": "ANDA", "marketing_start_date": "20190327", "listing_expiration_date": "20261231"}