Package 24658-797-01

Brand: doxepin hydrochloride

Generic: doxepin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24658-797-01
Digits Only 2465879701
Product NDC 24658-797
Description

100 CAPSULE in 1 BOTTLE (24658-797-01)

Marketing

Marketing Status
Marketed Since 2023-03-14
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": "14002bad-2577-436d-91ca-ec1b80ab0c97", "openfda": {"upc": ["0324658793016", "0324658797106", "0324658796017", "0324658794013", "0324658795010"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["14002bad-2577-436d-91ca-ec1b80ab0c97"], "manufacturer_name": ["PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (24658-797-01)", "package_ndc": "24658-797-01", "marketing_start_date": "20230314"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (24658-797-05)", "package_ndc": "24658-797-05", "marketing_start_date": "20230314"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (24658-797-10)", "package_ndc": "24658-797-10", "marketing_start_date": "20230314"}], "brand_name": "Doxepin Hydrochloride", "product_id": "24658-797_14002bad-2577-436d-91ca-ec1b80ab0c97", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "24658-797", "generic_name": "Doxepin Hydrochloride", "labeler_name": "PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA210675", "marketing_category": "ANDA", "marketing_start_date": "20230314", "listing_expiration_date": "20261231"}