NDC 72162-1490 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-1490

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 (1)

Package NDCDescriptionSince
72162-1490-5500 TABLET in 1 BOTTLE (72162-1490-5)Apr 21, 2023

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