Package 72789-220-30

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-220-30
Digits Only 7278922030
Product NDC 72789-220
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (72789-220-30)

Marketing

Marketing Status
Marketed Since 2021-12-22
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": "2ad0418c-56c4-50a0-e063-6394a90a35ca", "openfda": {"upc": ["0372789220307"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["2bf7d838-6274-4d8a-91cb-b27e1e81d273"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-220-30)", "package_ndc": "72789-220-30", "marketing_start_date": "20211222"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-220-90)", "package_ndc": "72789-220-90", "marketing_start_date": "20240906"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72789-220_2ad0418c-56c4-50a0-e063-6394a90a35ca", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-220", "generic_name": "Doxepin Hydrochloride", "labeler_name": "PD-Rx 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"}