Amidate - 52584-695-01 - (Etomidate)

Alphabetical Index


Drug Information of Amidate

Product NDC: 52584-695
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: 52584-695
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018227
Marketing Category: NDA
Start Marketing Date: 20100801

Package Information of Amidate

Package NDC: 52584-695-01
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (52584-695-01) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Amidate

NDC Code 52584-695-01
Proprietary Name Amidate
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (52584-695-01) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 52584-695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etomidate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100801
Marketing Category Name NDA
Labeler Name General Injectables & Vaccines, 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