Package 27241-167-10
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
27241-167-10
Digits Only
2724116710
Product NDC
27241-167
Description
1000 CAPSULE in 1 BOTTLE (27241-167-10)
Marketing
Marketing Status
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": "4f6891be-49a9-4884-a1ce-35e148c7c156", "openfda": {"upc": ["0327241167010", "0327241170010", "0327241171017", "0327241169014", "0327241168017"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["1513c98c-e7ef-4009-b932-6757048bb86a"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (27241-167-01)", "package_ndc": "27241-167-01", "marketing_start_date": "20191220"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (27241-167-10)", "package_ndc": "27241-167-10", "marketing_start_date": "20200220"}], "brand_name": "Doxepin hydrochloride", "product_id": "27241-167_4f6891be-49a9-4884-a1ce-35e148c7c156", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "27241-167", "generic_name": "Doxepin hydrochloride", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212624", "marketing_category": "ANDA", "marketing_start_date": "20191220", "listing_expiration_date": "20261231"}