Package 70518-3594-1
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
70518-3594-1
Digits Only
7051835941
Product NDC
70518-3594
Description
30 CAPSULE in 1 BLISTER PACK (70518-3594-1)
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": "43d02bba-f297-c107-e063-6294a90a6f92", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000048"], "spl_set_id": ["4ecd3b43-b5f1-4cf4-af36-eb214c1a3c60"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3594-1)", "package_ndc": "70518-3594-1", "marketing_start_date": "20250207"}], "brand_name": "Doxepin hydrochloride", "product_id": "70518-3594_43d02bba-f297-c107-e063-6294a90a6f92", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3594", "generic_name": "Doxepin hydrochloride", "labeler_name": "REMEDYREPACK 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": "20221213", "listing_expiration_date": "20261231"}