Home NDC 87722-092 apgwgzminoxidil5%
Product NDC 87722-092
11-digit product format 877220092
Labeler code 87722
Product ID 87722-092_596d0c4e-5eb9-bf37-e063-6394a90a157e
Type HUMAN OTC DRUG
Nonproprietary name minoxidil
Dosage form SOLUTION
Route TOPICAL
Labeler Guangdong Jiaoyu Biotechnology Co., Ltd
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-19
Substance MINOXIDIL
Active strength 5 mg/100mg
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base apgwgzminoxidil5%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5965120SH1 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311724 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 15 of 31 · 615 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87722-092-01 87722009201 25 mg in 1 BOTTLE (87722-092-01) 25 mg 2026-08-19 No No Current