Package 0378-8117-45

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-8117-45
Digits Only 0378811745
Product NDC 0378-8117
Product ID 0378-8117_b4771ea7-c19b-4182-bb23-c1473ab583fa
Description

1 TUBE in 1 CARTON (0378-8117-45) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-01-04
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": ["TOPICAL"], "spl_id": "b4771ea7-c19b-4182-bb23-c1473ab583fa", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000091"], "spl_set_id": ["b4771ea7-c19b-4182-bb23-c1473ab583fa"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0378-8117-45)  / 45 g in 1 TUBE", "package_ndc": "0378-8117-45", "marketing_start_date": "20190104"}], "brand_name": "Doxepin Hydrochloride", "product_id": "0378-8117_b4771ea7-c19b-4182-bb23-c1473ab583fa", "dosage_form": "CREAM", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0378-8117", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/g"}], "application_number": "NDA020126", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190104", "listing_expiration_date": "20261231"}