droxidopa
Generic: droxidopa
Labeler: slate run pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
droxidopa
Generic Name
droxidopa
Labeler
slate run pharmaceuticals, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
droxidopa 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70436-140
Product ID
70436-140_1af8aeac-14cf-4330-bf4e-3e50348268c1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215265
Listing Expiration
2026-12-31
Marketing Start
2021-11-10
Pharmacologic Class
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70436140
Hyphenated Format
70436-140
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
ANDA215265 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (70436-140-06)
Packages (1)
Ingredients (1)
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 (70436-140-06)", "package_ndc": "70436-140-06", "marketing_start_date": "20211110"}], "brand_name": "droxidopa", "product_id": "70436-140_1af8aeac-14cf-4330-bf4e-3e50348268c1", "dosage_form": "CAPSULE", "pharm_class": ["Catecholamines [CS]", "Increased Blood Pressure [PE]"], "product_ndc": "70436-140", "generic_name": "droxidopa", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "droxidopa", "active_ingredients": [{"name": "DROXIDOPA", "strength": "100 mg/1"}], "application_number": "ANDA215265", "marketing_category": "ANDA", "marketing_start_date": "20211110", "listing_expiration_date": "20261231"}