Amidate - 0409-6695-02 - (ETOMIDATE)

Alphabetical Index


Drug Information of Amidate

Product NDC: 0409-6695
Proprietary Name: Amidate
Non Proprietary Name: ETOMIDATE
Active Ingredient(s): 2    mg/mL & nbsp;   ETOMIDATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Amidate

Product NDC: 0409-6695
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018227
Marketing Category: NDA
Start Marketing Date: 20100210

Package Information of Amidate

Package NDC: 0409-6695-02
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Amidate

NDC Code 0409-6695-02
Proprietary Name Amidate
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6695-02) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-6695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ETOMIDATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100210
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name ETOMIDATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Amidate


General Information