NDC 63629-9433 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-9433

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071826
Marketed since
November 14, 1988
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
63629-9433-130 TABLET in 1 BOTTLE (63629-9433-1)Aug 20, 2026
63629-9433-290 TABLET in 1 BOTTLE (63629-9433-2)Aug 20, 2026
63629-9433-3100 TABLET in 1 BOTTLE (63629-9433-3)Aug 20, 2026
63629-9433-460 TABLET in 1 BOTTLE (63629-9433-4)Aug 20, 2026

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