Package 70518-0386-1
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
70518-0386-1
Digits Only
7051803861
Product NDC
70518-0386
Description
30 CAPSULE in 1 BLISTER PACK (70518-0386-1)
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": "47f546a1-56b1-7ba4-e063-6294a90a9a27", "openfda": {"unii": ["3U9A0FE9N5"], "rxcui": ["1000064"], "spl_set_id": ["0d981fbd-3605-417b-91d7-799b21c1a9e3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0386-1)", "package_ndc": "70518-0386-1", "marketing_start_date": "20230911"}], "brand_name": "Doxepin Hydrochloride", "product_id": "70518-0386_47f546a1-56b1-7ba4-e063-6294a90a9a27", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-0386", "generic_name": "Doxepin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxepin Hydrochloride", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA071669", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20271231"}