Package 0904-7053-61

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7053-61
Digits Only 0904705361
Product NDC 0904-7053
Product ID 0904-7053_b96f2236-46f3-47c4-a658-aa3d30f56b0c
Description

100 BLISTER PACK in 1 CARTON (0904-7053-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-06-28
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": "b96f2236-46f3-47c4-a658-aa3d30f56b0c", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076"], "spl_set_id": ["df3b6be0-6a64-4174-b351-dab2061f290e"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7053-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7053-61", "marketing_start_date": "20170628"}], "brand_name": "Doxepin Hydrochloride", "product_id": "0904-7053_b96f2236-46f3-47c4-a658-aa3d30f56b0c", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0904-7053", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA207482", "marketing_category": "ANDA", "marketing_start_date": "20170628", "listing_expiration_date": "20261231"}