NDC 63629-1086 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1086

Product details

Brand name
Minoxidil
Generic name
minoxidil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072709
Marketed since
December 14, 1995
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
63629-1086-1100 TABLET in 1 BOTTLE (63629-1086-1)Dec 14, 1995

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