NDC 0781-5668 – Voriconazole

Voriconazole 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0781-5668

Product details

Brand name
Voriconazole
Generic name
Voriconazole
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200265
Marketed since
December 12, 2011
Listing expires
December 31, 2027
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Voriconazole →

Package NDC codes (4)

Package NDCDescriptionSince
0781-5668-05500 TABLET, FILM COATED in 1 BOTTLE (0781-5668-05)Dec 12, 2011
0781-5668-101000 TABLET, FILM COATED in 1 BOTTLE (0781-5668-10)Dec 12, 2011
0781-5668-1310 BLISTER PACK in 1 CARTON (0781-5668-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5668-06)Dec 12, 2011
0781-5668-3130 TABLET, FILM COATED in 1 BOTTLE (0781-5668-31)Dec 12, 2011

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