NDCFind

Ciclopirox Olamine 51672-1318-08

Package NDC

51672-1318-08

Product NDC: 51672-1318

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Cream
Route
Topical
Product Type
Human Prescription Drug
Marketing Start
April 12, 2005
Listing Expires
December 31, 2027
Application
ANDA076790
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Active Ingredients

IngredientStrength
Ciclopirox Olamine7.7 mg/g

Drug Class

Decreased DNA Replication [PE]Decreased Protein Synthesis [PE]Decreased RNA Replication [PE]

Selected Package

51672-1318-08Selected

1 TUBE in 1 CARTON (51672-1318-8) / 90 g in 1 TUBE

Other packages for this product(2)

1 TUBE in 1 CARTON (51672-1318-1) / 15 g in 1 TUBE

1 TUBE in 1 CARTON (51672-1318-2) / 30 g in 1 TUBE