Ketoconazole 51672-4026-08
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 15, 1999
- Listing Expires
- December 31, 2026
- Application
- ANDA075319
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ketoconazole | 200 mg/1 |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Selected Package
51672-4026-08Selected3 BLISTER PACK in 1 BOX (51672-4026-8) / 10 TABLET in 1 BLISTER PACK
Other packages for this product(5)
10 BLISTER PACK in 1 BOX (51672-4026-0) / 10 TABLET in 1 BLISTER PACK
100 TABLET in 1 BOTTLE (51672-4026-1)
500 TABLET in 1 BOTTLE (51672-4026-2)
30 TABLET in 1 BOTTLE (51672-4026-6)
5 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACK