NDC 42192-715 – Ciclopirox

Ciclopirox 80 mg/mL · Solution · Topical

Human Prescription Drug

Product NDC42192-715

Product details

Brand name
Ciclopirox
Generic name
Ciclopirox
Labeler
Acella Pharmaceuticals, LLC
Dosage form
Solution
Route
Topical
Marketing category
ANDA · ANDA078172
Marketed since
November 4, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Ciclopirox →

Package NDC codes (1)

Package NDCDescriptionSince
42192-715-061 BOTTLE in 1 CARTON (42192-715-06) / 6.6 mL in 1 BOTTLENov 4, 2019

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