NDC 71205-757 – Minoxidil

Minoxidil 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-757

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071344
Marketed since
October 26, 2009
Listing expires
December 31, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (3)

Package NDCDescriptionSince
71205-757-3030 TABLET in 1 BOTTLE, PLASTIC (71205-757-30)Feb 7, 2023
71205-757-6060 TABLET in 1 BOTTLE, PLASTIC (71205-757-60)Feb 7, 2023
71205-757-9090 TABLET in 1 BOTTLE, PLASTIC (71205-757-90)Feb 7, 2023

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