NDC 71335-3174 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3174

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071344
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 (4)

Package NDCDescriptionSince
71335-3174-130 TABLET in 1 BOTTLE (71335-3174-1)Aug 20, 2026
71335-3174-290 TABLET in 1 BOTTLE (71335-3174-2)Aug 20, 2026
71335-3174-3100 TABLET in 1 BOTTLE (71335-3174-3)Aug 20, 2026
71335-3174-460 TABLET in 1 BOTTLE (71335-3174-4)Aug 20, 2026

Other Minoxidil products