NDC 82804-240 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-240

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071826
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
82804-240-3030 TABLET in 1 BOTTLE (82804-240-30)Sep 5, 2025

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