NDC 71335-3120 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3120

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071345
Marketed since
October 26, 2009
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (2)

Package NDCDescriptionSince
71335-3120-1100 TABLET in 1 BOTTLE (71335-3120-1)Apr 13, 2026
71335-3120-230 TABLET in 1 BOTTLE (71335-3120-2)Apr 13, 2026

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