Package 54838-512-40

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54838-512-40
Digits Only 5483851240
Product NDC 54838-512
Product ID 54838-512_5408fdf5-16a7-4d5a-b4c4-2ccb271759a2
Description

120 mL in 1 BOTTLE, PLASTIC (54838-512-40)

Marketing

Marketing Status
Marketed Since 1998-12-29
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": "5408fdf5-16a7-4d5a-b4c4-2ccb271759a2", "openfda": {"upc": ["0354838512403"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000054"], "spl_set_id": ["f350afed-120b-422d-9e6e-3aaa0f72a5fb"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (54838-512-40)", "package_ndc": "54838-512-40", "marketing_start_date": "19981229"}], "brand_name": "Doxepin Hydrochloride", "product_id": "54838-512_5408fdf5-16a7-4d5a-b4c4-2ccb271759a2", "dosage_form": "SOLUTION", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "54838-512", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA074721", "marketing_category": "ANDA", "marketing_start_date": "19981229", "listing_expiration_date": "20261231"}