Package 50090-7184-1

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7184-1
Digits Only 5009071841
Product NDC 50090-7184
Product ID 50090-7184_7bd0f29d-ffc3-496b-9fd7-16345aa76356
Description

30 CAPSULE in 1 BOTTLE (50090-7184-1)

Marketing

Marketing Status
Marketed Since 2024-06-18
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": "7bd0f29d-ffc3-496b-9fd7-16345aa76356", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000076"], "spl_set_id": ["890248d7-73b1-4ed3-b252-85775defdf34"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7184-1)", "package_ndc": "50090-7184-1", "marketing_start_date": "20240618"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "50090-7184_7bd0f29d-ffc3-496b-9fd7-16345aa76356", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-7184", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}