Package 64980-598-01
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
64980-598-01
Digits Only
6498059801
Product NDC
64980-598
Description
100 CAPSULE in 1 BOTTLE (64980-598-01)
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": "2877d1f2-a036-4577-926d-b09828350ea1", "openfda": {"upc": ["0364980594011", "0364980597012", "0364980595018", "0364980596015", "0364980598019"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["66c6af99-9909-4b18-a43b-898a1c4a34d7"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (64980-598-01)", "package_ndc": "64980-598-01", "marketing_start_date": "20231225"}], "brand_name": "Doxepin hydrochloride", "product_id": "64980-598_2877d1f2-a036-4577-926d-b09828350ea1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "64980-598", "generic_name": "Doxepin hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA217975", "marketing_category": "ANDA", "marketing_start_date": "20231225", "listing_expiration_date": "20261231"}