Fluocinolone Acetonide 51672-1357
Product NDC
51672-1357- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Oil
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- May 19, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA209336
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluocinolone Acetonide | .11 mg/118.28mL |
Drug Class
Corticosteroid [EPC]Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
1 BOTTLE in 1 CARTON (51672-1357-8) / 118.28 mL in 1 BOTTLE