Package 69238-1733-6

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69238-1733-6
Digits Only 6923817336
Product NDC 69238-1733
Product ID 69238-1733_f44f392e-0f43-4e5d-a2c4-0b15387d67ac
Description

1 TUBE in 1 CARTON (69238-1733-6) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-08-21
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": "f44f392e-0f43-4e5d-a2c4-0b15387d67ac", "openfda": {"upc": ["0369238173369"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000091"], "spl_set_id": ["dd8d5edd-7b08-4061-86e6-c4179da89c0d"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69238-1733-6)  / 45 g in 1 TUBE", "package_ndc": "69238-1733-6", "marketing_start_date": "20230821"}], "brand_name": "Doxepin Hydrochloride", "product_id": "69238-1733_f44f392e-0f43-4e5d-a2c4-0b15387d67ac", "dosage_form": "CREAM", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "69238-1733", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/g"}], "application_number": "ANDA212357", "marketing_category": "ANDA", "marketing_start_date": "20230821", "listing_expiration_date": "20261231"}