Package 70436-141-06

Brand: droxidopa

Generic: droxidopa
NDC Package

Package Facts

Identity

Package NDC 70436-141-06
Digits Only 7043614106
Product NDC 70436-141
Description

90 CAPSULE in 1 BOTTLE (70436-141-06)

Marketing

Marketing Status
Marketed Since 2021-11-10
Brand droxidopa
Generic droxidopa
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1af8aeac-14cf-4330-bf4e-3e50348268c1", "openfda": {"nui": ["M0003647", "N0000178478"], "unii": ["J7A92W69L7"], "rxcui": ["1490026", "1490034", "1490038"], "spl_set_id": ["049f997b-1649-467e-bbb9-bdb991b0bc6e"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_pe": ["Increased Blood Pressure [PE]"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (70436-141-06)", "package_ndc": "70436-141-06", "marketing_start_date": "20211110"}], "brand_name": "droxidopa", "product_id": "70436-141_1af8aeac-14cf-4330-bf4e-3e50348268c1", "dosage_form": "CAPSULE", "pharm_class": ["Catecholamines [CS]", "Increased Blood Pressure [PE]"], "product_ndc": "70436-141", "generic_name": "droxidopa", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "droxidopa", "active_ingredients": [{"name": "DROXIDOPA", "strength": "200 mg/1"}], "application_number": "ANDA215265", "marketing_category": "ANDA", "marketing_start_date": "20211110", "listing_expiration_date": "20261231"}