droxidopa
Generic: droxidopa
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
droxidopa
Generic Name
droxidopa
Labeler
aurobindo pharma limited
Dosage Form
CAPSULE
Routes
Active Ingredients
droxidopa 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-376
Product ID
59651-376_eb94f573-c790-4392-95a4-ff99a81a181f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214387
Listing Expiration
2026-12-31
Marketing Start
2021-02-18
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651376
Hyphenated Format
59651-376
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
droxidopa (source: ndc)
Generic Name
droxidopa (source: ndc)
Application Number
ANDA214387 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (59651-376-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb94f573-c790-4392-95a4-ff99a81a181f", "openfda": {"nui": ["M0003647", "N0000178478"], "unii": ["J7A92W69L7"], "rxcui": ["1490026", "1490034", "1490038"], "spl_set_id": ["ff263c9a-3db2-45ac-9ba6-8fca47199604"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_pe": ["Increased Blood Pressure [PE]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (59651-376-90)", "package_ndc": "59651-376-90", "marketing_start_date": "20210218"}], "brand_name": "Droxidopa", "product_id": "59651-376_eb94f573-c790-4392-95a4-ff99a81a181f", "dosage_form": "CAPSULE", "pharm_class": ["Catecholamines [CS]", "Increased Blood Pressure [PE]"], "product_ndc": "59651-376", "generic_name": "Droxidopa", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Droxidopa", "active_ingredients": [{"name": "DROXIDOPA", "strength": "200 mg/1"}], "application_number": "ANDA214387", "marketing_category": "ANDA", "marketing_start_date": "20210218", "listing_expiration_date": "20261231"}