Betamethasone Dipropionate 51672-1310
Product NDC
51672-1310- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream, Augmented
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- December 9, 2003
- Listing Expires
- December 31, 2026
- Application
- ANDA076543
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Betamethasone Dipropionate | .5 mg/g |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(3)
1 TUBE in 1 CARTON (51672-1310-1) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1310-2) / 30 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1310-3) / 50 g in 1 TUBE