Package 59651-844-30

Brand: doxepin

Generic: doxepin
NDC Package

Package Facts

Identity

Package NDC 59651-844-30
Digits Only 5965184430
Product NDC 59651-844
Product ID 59651-844_29b3bf98-2c57-4d87-b5eb-5232e46dc639
Description

30 TABLET in 1 BOTTLE (59651-844-30)

Marketing

Marketing Status
Marketed Since 2025-07-12
Brand doxepin
Generic doxepin
Sample Package No

Linked Drug Pages (1)

DOXEPIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "29b3bf98-2c57-4d87-b5eb-5232e46dc639", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["29b3bf98-2c57-4d87-b5eb-5232e46dc639"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (59651-844-30)", "package_ndc": "59651-844-30", "marketing_start_date": "20250712"}], "brand_name": "DOXEPIN", "product_id": "59651-844_29b3bf98-2c57-4d87-b5eb-5232e46dc639", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "59651-844", "generic_name": "DOXEPIN", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA216041", "marketing_category": "ANDA", "marketing_start_date": "20250712", "listing_expiration_date": "20261231"}