NDC 68462-573 – Voriconazole
Voriconazole 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-573
Product details
- Brand name
- Voriconazole
- Generic name
- Voriconazole
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203503
- Marketed since
- September 4, 2015
- Marketing end
- January 1, 2027
- Pharmacologic class
- Azole Antifungal
Active ingredients
- Voriconazole 200 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-573-13 | 3 BLISTER PACK in 1 CARTON (68462-573-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 4, 2015 |
| 68462-573-30 | 30 TABLET, FILM COATED in 1 BOTTLE (68462-573-30) | Sep 4, 2015 |
| 68462-573-90 | 90 TABLET, FILM COATED in 1 BOTTLE (68462-573-90) | Sep 4, 2015 |
Recalls mentioning this NDC
- D-0319-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-0318-2025 Apr 16, 2025 · Class II
CGMP Deviations
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