Betamethasone Dipropionate 51672-1309-01

Package NDC

51672-1309-01

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Gel
Route: Topical
Product Type: Human Prescription Drug
Marketing Start: December 2, 2003
Listing Expires: December 31, 2026
Application: ANDA076508

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Active Ingredients

Ingredient	Strength
Betamethasone Dipropionate	.5 mg/g

Drug Class

Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]

Selected Package

51672-1309-01Selected

1 TUBE in 1 CARTON (51672-1309-1) / 15 g in 1 TUBE

Other packages for this product(1)

51672-1309-03

1 TUBE in 1 CARTON (51672-1309-3) / 50 g in 1 TUBE

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