Betamethasone Dipropionate 51672-1340
Product NDC
51672-1340- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Lotion, Augmented
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- May 21, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077477
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Betamethasone Dipropionate | .5 mg/mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(2)
1 BOTTLE in 1 CARTON (51672-1340-3) / 30 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON (51672-1340-4) / 60 mL in 1 BOTTLE