Package 55801-529-02

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55801-529-02
Digits Only 5580152902
Product NDC 55801-529
Description

500 CAPSULE in 1 BOTTLE (55801-529-02)

Marketing

Marketing Status
Marketed Since 2021-06-01
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": "897d1512-3e1a-469e-bcb9-131e514ed562", "openfda": {"upc": ["0355801529015", "0355801530028", "0355801527011", "0355801528025"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["abf4c515-8888-4733-80a0-fd4e1cdb84a2"], "manufacturer_name": ["Appco Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (55801-529-01)", "package_ndc": "55801-529-01", "marketing_start_date": "20210601"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (55801-529-02)", "package_ndc": "55801-529-02", "marketing_start_date": "20210601"}], "brand_name": "Doxepin Hydrochloride", "product_id": "55801-529_897d1512-3e1a-469e-bcb9-131e514ed562", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "55801-529", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Appco Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214908", "marketing_category": "ANDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}