NDC 63629-9620 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-9620

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071839
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 (2)

Package NDCDescriptionSince
63629-9620-1100 TABLET in 1 BOTTLE (63629-9620-1)Mar 27, 2023
63629-9620-230 TABLET in 1 BOTTLE (63629-9620-2)Mar 27, 2023

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