Package 71921-166-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71921-166-01
Digits Only 7192116601
Product NDC 71921-166
Product ID 71921-166_ccbb860e-6367-5114-e053-2a95a90abfb9
Description

100 CAPSULE in 1 BOTTLE (71921-166-01)

Marketing

Marketing Status
Marketed Since 2021-05-01
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": "ccbb860e-6367-5114-e053-2a95a90abfb9", "openfda": {"upc": ["0371921162017", "0371921164011", "0371921163014", "0371921166015", "0371921165018"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["b787a283-f882-e1f0-e053-2a95a90a8975"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71921-166-01)", "package_ndc": "71921-166-01", "marketing_start_date": "20210501"}], "brand_name": "Doxepin Hydrochloride", "product_id": "71921-166_ccbb860e-6367-5114-e053-2a95a90abfb9", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71921-166", "generic_name": "Doxepin Hydrochloride", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA213474", "marketing_category": "ANDA", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}