Package 67296-2165-2

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2165-2
Digits Only 6729621652
Product NDC 67296-2165
Product ID 67296-2165_45abebda-9f37-adae-e063-6294a90a811a
Description

20 CAPSULE in 1 BOTTLE (67296-2165-2)

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": "45abebda-9f37-adae-e063-6294a90a811a", "openfda": {"upc": ["0369238117134"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["37451a61-ccb1-57b3-e063-6294a90a2592"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (67296-2165-2)", "package_ndc": "67296-2165-2", "marketing_start_date": "20170628"}], "brand_name": "Doxepin Hydrochloride", "product_id": "67296-2165_45abebda-9f37-adae-e063-6294a90a811a", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "67296-2165", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207482", "marketing_category": "ANDA", "marketing_start_date": "20170628", "listing_expiration_date": "20261231"}