Package 72789-542-30

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-542-30
Digits Only 7278954230
Product NDC 72789-542
Product ID 72789-542_463de429-bc73-951e-e063-6394a90add02
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (72789-542-30)

Marketing

Marketing Status
Marketed Since 2025-12-18
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": "463de429-bc73-951e-e063-6394a90add02", "openfda": {"upc": ["0372789542300"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000070"], "spl_set_id": ["1496dfc1-de50-471c-be87-1f1e2b70ab5a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-542-30)", "package_ndc": "72789-542-30", "marketing_start_date": "20251218"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72789-542_463de429-bc73-951e-e063-6394a90add02", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72789-542", "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": "25 mg/1"}], "application_number": "ANDA211603", "marketing_category": "ANDA", "marketing_start_date": "20190327", "listing_expiration_date": "20261231"}