Package 44183-106-30
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
44183-106-30
Digits Only
4418310630
Product NDC
44183-106
Description
30 TABLET in 1 BOTTLE (44183-106-30)
Marketing
Marketing Status
Brand
doxepin hydrochloride
Generic
doxepin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db184464-82a3-4710-a6aa-6a1c437a7bfc", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["5b4dba99-6b66-4091-94f1-bf5f021c688a"], "manufacturer_name": ["Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (44183-106-30)", "package_ndc": "44183-106-30", "marketing_start_date": "20100801"}], "brand_name": "doxepin hydrochloride", "product_id": "44183-106_db184464-82a3-4710-a6aa-6a1c437a7bfc", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "44183-106", "generic_name": "doxepin hydrochloride", "labeler_name": "Currax Pharmaceuticals LLC dba Cypress, Hawthorn, Macoven", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "NDA022036", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20100801", "listing_expiration_date": "20261231"}