Package 64380-203-02

Brand: doxepin

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64380-203-02
Digits Only 6438020302
Product NDC 64380-203
Product ID 64380-203_b6b0f575-6e3a-4011-b33f-a051103058c2
Description

100 TABLET in 1 BOTTLE, PLASTIC (64380-203-02)

Marketing

Marketing Status
Marketed Since 2022-09-12
Brand doxepin
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Doxepin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b6b0f575-6e3a-4011-b33f-a051103058c2", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["966787", "966793"], "spl_set_id": ["399866d5-3fa6-46d0-9c62-492d5997bc4f"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (64380-203-01)", "package_ndc": "64380-203-01", "marketing_start_date": "20220912"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (64380-203-02)", "package_ndc": "64380-203-02", "marketing_start_date": "20220912"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (64380-203-03)", "package_ndc": "64380-203-03", "marketing_start_date": "20220912"}], "brand_name": "Doxepin", "product_id": "64380-203_b6b0f575-6e3a-4011-b33f-a051103058c2", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "64380-203", "generic_name": "doxepin hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA202510", "marketing_category": "ANDA", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}