Package 51672-4247-2

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-4247-2
Digits Only 5167242472
Product NDC 51672-4247
Product ID 51672-4247_36adb81c-3442-17dc-e063-6394a90aaafa
Description

30 TABLET in 1 BOTTLE (51672-4247-2)

Marketing

Marketing Status
Marketed Since 2025-08-07
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": "36adb81c-3442-17dc-e063-6394a90aaafa", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["554ab06f-6420-42b3-89d1-d97554c237d8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (51672-4247-2)", "package_ndc": "51672-4247-2", "marketing_start_date": "20250807"}], "brand_name": "doxepin hydrochloride", "product_id": "51672-4247_36adb81c-3442-17dc-e063-6394a90aaafa", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51672-4247", "generic_name": "doxepin hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA219058", "marketing_category": "ANDA", "marketing_start_date": "20250807", "listing_expiration_date": "20261231"}