Ketoconazole 72789-0052
Product NDC
72789-0052- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 26, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA210457
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ketoconazole | 200 mg/1 |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(1)
30 TABLET in 1 BOTTLE, PLASTIC (72789-052-30)