Package 49884-222-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-222-01
Digits Only 4988422201
Product NDC 49884-222
Product ID 49884-222_75a2a220-95ff-4c6a-aa58-15e3352b6e7f
Description

100 CAPSULE in 1 BOTTLE (49884-222-01)

Marketing

Marketing Status
Marketed Since 1987-11-09
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": "75a2a220-95ff-4c6a-aa58-15e3352b6e7f", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000064"], "spl_set_id": ["71cff7cd-0410-4194-9cdd-af404a869edd"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-222-01)", "package_ndc": "49884-222-01", "marketing_start_date": "19871109"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (49884-222-03)", "package_ndc": "49884-222-03", "marketing_start_date": "19871109"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (49884-222-05)", "package_ndc": "49884-222-05", "marketing_start_date": "19871109"}], "brand_name": "Doxepin Hydrochloride", "product_id": "49884-222_75a2a220-95ff-4c6a-aa58-15e3352b6e7f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "49884-222", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA071422", "marketing_category": "ANDA", "marketing_start_date": "19871109", "listing_expiration_date": "20261231"}