Package 43353-329-09

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43353-329-09
Digits Only 4335332909
Product NDC 43353-329
Description

9000 CAPSULE in 1 BOTTLE, PLASTIC (43353-329-09)

Marketing

Marketing Status
Marketed Since 2017-05-21
Brand doxepin hydrochloride
Generic doxepin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a3797445-680f-449e-8ffd-522445906bdb", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000070"], "spl_set_id": ["10d9eba6-30d1-448a-8d92-a1a02df03303"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 CAPSULE in 1 BOTTLE, PLASTIC (43353-329-09)", "package_ndc": "43353-329-09", "marketing_start_date": "20170521"}], "brand_name": "Doxepin Hydrochloride", "product_id": "43353-329_a3797445-680f-449e-8ffd-522445906bdb", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "43353-329", "generic_name": "doxepin hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070791", "marketing_category": "ANDA", "marketing_start_date": "19860513", "listing_expiration_date": "20261231"}