opusmeds extra strength minoxidil
Generic: minoxidil
Labeler: opus meds llcDrug Facts
Product Profile
Brand Name
opusmeds extra strength minoxidil
Generic Name
minoxidil
Labeler
opus meds llc
Dosage Form
SOLUTION
Routes
Active Ingredients
minoxidil 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
87338-983
Product ID
87338-983_494a6bca-19c5-f856-e063-6294a90ab251
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076239
Listing Expiration
2027-12-31
Marketing Start
2026-01-06
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
87338983
Hyphenated Format
87338-983
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
opusmeds extra strength minoxidil (source: ndc)
Generic Name
minoxidil (source: ndc)
Application Number
ANDA076239 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 1 BOTTLE, DROPPER in 1 BOX (87338-983-00) / 60 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "494a6bca-19c5-f856-e063-6294a90ab251", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["311724"], "spl_set_id": ["eab00b6d-d49a-4090-8243-ae5e99f6a54e"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Opus Meds LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 BOX (87338-983-00) / 60 mL in 1 BOTTLE, DROPPER", "package_ndc": "87338-983-00", "marketing_start_date": "20260106"}], "brand_name": "OpusMeds Extra Strength Minoxidil", "product_id": "87338-983_494a6bca-19c5-f856-e063-6294a90ab251", "dosage_form": "SOLUTION", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "87338-983", "generic_name": "MINOXIDIL", "labeler_name": "Opus Meds LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OpusMeds Extra Strength Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/mL"}], "application_number": "ANDA076239", "marketing_category": "ANDA", "marketing_start_date": "20260106", "listing_expiration_date": "20271231"}