Acetazolamide

ACETAZOLAMIDE — acetazolamide sodium injection, powder, lyophilized, for solution
Cadila Healthcare Limited

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Container Label

NDC 70771-1490-1

AcetaZOLAMIDE for Injection USP

500 mg* per vial

For Intravenous Use

1 Single-Dose Vial

Rx Only

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(click image for full-size original)

Carton Label

NDC 70771-1490-1

AcetaZOLAMIDE for Injection USP

500 mg* per vial

For Intravenous Use

1 Single-Dose Vial

Rx Only

figure03
(click image for full-size original)
ACETAZOLAMIDE
acetazolamide injection, powder, lyophilized, for solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70771-1490
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAZOLAMIDE SODIUM (ACETAZOLAMIDE) ACETAZOLAMIDE 500 mg in 5 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM HYDROXIDE
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70771-1490-1 1 VIAL in 1 CARTON contains a VIAL
1 5 mL in 1 VIAL This package is contained within the CARTON (70771-1490-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA206533 01/09/2020
Labeler — Cadila Healthcare Limited (918596198)
Registrant — Cadila Healthcare Limited (918596198)
Establishment
Name Address ID/FEI Operations
Cadila Healthcare Limited 918596198 ANALYSIS (70771-1490), MANUFACTURE (70771-1490)

Revised: 12/2020 Cadila Healthcare Limited

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