Package 0093-9609-95

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-9609-95
Digits Only 0093960995
Product NDC 0093-9609
Product ID 0093-9609_7d22a419-3d33-492c-b054-fb29a82ce643
Description

1 TUBE in 1 CARTON (0093-9609-95) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-02-17
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": "7d22a419-3d33-492c-b054-fb29a82ce643", "openfda": {"upc": ["0300939609955"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000091"], "spl_set_id": ["4a4eab1c-8e19-48f5-9216-09ab83eaa5f8"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0093-9609-95)  / 45 g in 1 TUBE", "package_ndc": "0093-9609-95", "marketing_start_date": "20230217"}], "brand_name": "doxepin hydrochloride", "product_id": "0093-9609_7d22a419-3d33-492c-b054-fb29a82ce643", "dosage_form": "CREAM", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0093-9609", "generic_name": "doxepin hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/g"}], "application_number": "ANDA215408", "marketing_category": "ANDA", "marketing_start_date": "20230217", "listing_expiration_date": "20261231"}