Voriconazole (Page 13 of 13)

PRINCIPAL DISPLAY PANEL – Voriconazole for Injection, 200 mg Container Label

NDC 71288-027 -30

Rx only

Voriconazole for Injection

200 mg* per vial

200 mg* of voriconazole

For Intravenous Infusion Only

Single-Dose Vial

Discard Unused Portion

PRINCIPAL DISPLAY PANEL – Voriconazole for Injection, 200 mg Container Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL – Voriconazole for Injection, 200 mg Carton

NDC 71288-027 -30

Rx only

Voriconazole for Injection

200 mg* per vial

200 mg* of voriconazole

For Intravenous Infusion Only

1 Single-Dose Vial

Discard Unused Portion

PRINCIPAL DISPLAY PANEL – Voriconazole for Injection, 200 mg Carton
(click image for full-size original)
VORICONAZOLE voriconazole injection, powder, lyophilized, for solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71288-027
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Voriconazole (Voriconazole) Voriconazole 10 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
betadex sulfobutyl ether sodium
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71288-027-30 1 VIAL, SINGLE-DOSE in 1 CARTON contains a VIAL, SINGLE-DOSE
1 20 mL in 1 VIAL, SINGLE-DOSE This package is contained within the CARTON (71288-027-30)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA214516 05/09/2022
Labeler — Meitheal Pharmaceuticals Inc. (080548348)

Revised: 10/2022 Meitheal Pharmaceuticals Inc.

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