droxidopa
Generic: droxidopa
Labeler: civicascript llcDrug Facts
Product Profile
Brand Name
droxidopa
Generic Name
droxidopa
Labeler
civicascript llc
Dosage Form
CAPSULE
Routes
Active Ingredients
droxidopa 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82249-554
Product ID
82249-554_f6dce609-c7d7-48a3-83bb-32ecf00f973f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213911
Listing Expiration
2026-12-31
Marketing Start
2025-03-03
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82249554
Hyphenated Format
82249-554
Supplemental Identifiers
RxCUI
UPC
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
ANDA213911 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (82249-554-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6dce609-c7d7-48a3-83bb-32ecf00f973f", "openfda": {"nui": ["M0003647", "N0000178478"], "upc": ["0382249554903"], "unii": ["J7A92W69L7"], "rxcui": ["1490026", "1490034", "1490038"], "spl_set_id": ["f6dce609-c7d7-48a3-83bb-32ecf00f973f"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_pe": ["Increased Blood Pressure [PE]"], "manufacturer_name": ["CivicaScript LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (82249-554-90)", "package_ndc": "82249-554-90", "marketing_start_date": "20250303"}], "brand_name": "Droxidopa", "product_id": "82249-554_f6dce609-c7d7-48a3-83bb-32ecf00f973f", "dosage_form": "CAPSULE", "pharm_class": ["Catecholamines [CS]", "Increased Blood Pressure [PE]"], "product_ndc": "82249-554", "generic_name": "Droxidopa", "labeler_name": "CivicaScript LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Droxidopa", "active_ingredients": [{"name": "DROXIDOPA", "strength": "300 mg/1"}], "application_number": "ANDA213911", "marketing_category": "ANDA", "marketing_start_date": "20250303", "listing_expiration_date": "20261231"}