Azelaic Acid 51672-1389-03

Package NDC

51672-1389-03

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Gel
Route: Topical
Product Type: Human Prescription Drug
Marketing Start: August 23, 2019
Listing Expires: December 31, 2026
Application: ANDA210549

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Active Ingredients

Ingredient	Strength
Azelaic Acid	.15 g/g

Drug Class

Decreased Protein Synthesis [PE]Decreased Sebaceous Gland Activity [PE]

Selected Package

51672-1389-03Selected

1 TUBE in 1 CARTON (51672-1389-3) / 50 g in 1 TUBE