Package 72603-394-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-394-01
Digits Only 7260339401
Product NDC 72603-394
Product ID 72603-394_ab6741eb-c631-4c5c-b06c-85b2333a1163
Description

100 CAPSULE in 1 BOTTLE (72603-394-01)

Marketing

Marketing Status
Marketed Since 2025-05-01
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": "ab6741eb-c631-4c5c-b06c-85b2333a1163", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["03cef3a6-a63d-4082-a491-451b24227d9d"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72603-394-01)", "package_ndc": "72603-394-01", "marketing_start_date": "20250501"}], "brand_name": "Doxepin Hydrochloride", "product_id": "72603-394_ab6741eb-c631-4c5c-b06c-85b2333a1163", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72603-394", "generic_name": "doxepin hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA215710", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}