NDC 0574-0611 – Podofilox

Podofilox 5 mg/mL · Solution · Topical

Human Prescription Drug 1 recall

Product NDC0574-0611

Product details

Brand name
Podofilox
Generic name
Podofilox
Labeler
Padagis US LLC
Dosage form
Solution
Route
Topical
Marketing category
ANDA · ANDA075600
Marketed since
January 29, 2002
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Podofilox →

Package NDC codes (1)

Package NDCDescriptionSince
0574-0611-051 BOTTLE, GLASS in 1 CARTON (0574-0611-05) / 3.5 mL in 1 BOTTLE, GLASSJan 29, 2002

Recalls mentioning this NDC

Other Podofilox products