Package 70710-1389-9

Brand: droxidopa

Generic: droxidopa
NDC Package

Package Facts

Identity

Package NDC 70710-1389-9
Digits Only 7071013899
Product NDC 70710-1389
Description

90 CAPSULE in 1 BOTTLE (70710-1389-9)

Marketing

Marketing Status
Marketed Since 2021-02-19
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": "98a2a992-f0a2-47e4-91c0-bdae39b73e63", "openfda": {"nui": ["M0003647", "N0000178478"], "unii": ["J7A92W69L7"], "rxcui": ["1490026", "1490034", "1490038"], "spl_set_id": ["aa3ce55a-1ea9-4b50-b682-6f25398bcc29"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_pe": ["Increased Blood Pressure [PE]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (70710-1389-9)", "package_ndc": "70710-1389-9", "marketing_start_date": "20210219"}], "brand_name": "Droxidopa", "product_id": "70710-1389_98a2a992-f0a2-47e4-91c0-bdae39b73e63", "dosage_form": "CAPSULE", "pharm_class": ["Catecholamines [CS]", "Increased Blood Pressure [PE]"], "product_ndc": "70710-1389", "generic_name": "Droxidopa", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Droxidopa", "active_ingredients": [{"name": "DROXIDOPA", "strength": "100 mg/1"}], "application_number": "ANDA211818", "marketing_category": "ANDA", "marketing_start_date": "20210219", "listing_expiration_date": "20261231"}