NDC 51407-902 – Minoxidil

Minoxidil 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51407-902

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Golden State Medical Supply, Inc.
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
51407-902-01100 TABLET in 1 BOTTLE (51407-902-01)Jul 11, 2024

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