NDC 51672-4026 – Ketoconazole
Ketoconazole 200 mg/1 · Tablet · Oral
Product NDC51672-4026
Product details
- Brand name
- Ketoconazole
- Generic name
- Ketoconazole
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075319
- Marketed since
- June 15, 1999
- Listing expires
- December 31, 2026
- Pharmacologic class
- Azole Antifungal
Active ingredients
- Ketoconazole 200 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4026-0 | 10 BLISTER PACK in 1 BOX (51672-4026-0) / 10 TABLET in 1 BLISTER PACK | Jun 15, 1999 |
| 51672-4026-1 | 100 TABLET in 1 BOTTLE (51672-4026-1) | Jun 15, 1999 |
| 51672-4026-2 | 500 TABLET in 1 BOTTLE (51672-4026-2) | Jun 15, 1999 |
| 51672-4026-8 | 3 BLISTER PACK in 1 BOX (51672-4026-8) / 10 TABLET in 1 BLISTER PACK | Jun 15, 1999 |
| 51672-4026-9 | 5 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACK | Jun 15, 1999 |
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