Dapsone 51672-1388
Product NDC
51672-1388- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Gel
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- June 26, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA210191
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dapsone | 75 mg/g |
Drug Class
Sulfone [EPC]Sulfone [EPC]Sulfones [CS]
Packaging Options(3)
1 BOTTLE, PUMP in 1 CARTON (51672-1388-2) / 30 g in 1 BOTTLE, PUMP
1 BOTTLE, PUMP in 1 CARTON (51672-1388-3) / 60 g in 1 BOTTLE, PUMP
1 BOTTLE, PUMP in 1 CARTON (51672-1388-8) / 90 g in 1 BOTTLE, PUMP