Package 59651-176-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-176-01
Digits Only 5965117601
Product NDC 59651-176
Product ID 59651-176_5b5efe70-cce2-4950-94f0-d3aa869e442e
Description

100 CAPSULE in 1 BOTTLE (59651-176-01)

Marketing

Marketing Status
Marketed Since 2019-03-27
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": "5b5efe70-cce2-4950-94f0-d3aa869e442e", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["f3c242dd-426e-4c69-8f21-2645361d5f27"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (59651-176-01)", "package_ndc": "59651-176-01", "marketing_start_date": "20190327"}], "brand_name": "Doxepin Hydrochloride", "product_id": "59651-176_5b5efe70-cce2-4950-94f0-d3aa869e442e", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "59651-176", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA211603", "marketing_category": "ANDA", "marketing_start_date": "20190327", "listing_expiration_date": "20261231"}