NDC 50090-7760 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7760

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071839
Marketed since
November 14, 1988
Listing expires
December 31, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (1)

Package NDCDescriptionSince
50090-7760-290 TABLET in 1 BOTTLE (50090-7760-2)Nov 6, 2025

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