Package 51407-812-30
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
51407-812-30
Digits Only
5140781230
Product NDC
51407-812
Description
30 TABLET in 1 BOTTLE (51407-812-30)
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": "2a07fb40-8690-5729-e063-6294a90a4078", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["00ef7d0b-4bb9-cd5b-e063-6294a90abc35"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (51407-812-30)", "package_ndc": "51407-812-30", "marketing_start_date": "20230531"}], "brand_name": "Doxepin hydrochloride", "product_id": "51407-812_2a07fb40-8690-5729-e063-6294a90a4078", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51407-812", "generic_name": "Doxepin hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "6 mg/1"}], "application_number": "ANDA214823", "marketing_category": "ANDA", "marketing_start_date": "20230405", "listing_expiration_date": "20261231"}