NDC 51662-1542

ETOMIDATE

Etomidate

ETOMIDATE is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Etomidate.

Product ID51662-1542_dc43b289-4f33-1c1e-e053-2995a90a3a23
NDC51662-1542
Product TypeHuman Prescription Drug
Proprietary NameETOMIDATE
Generic NameEtomidate
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-04-09
Marketing CategoryANDA /
Application NumberANDA206126
Labeler NameHF Acquisition Co LLC, DBA HealthFirst
Substance NameETOMIDATE
Active Ingredient Strength40 mg/20mL
Pharm ClassesGeneral Anesthesia [PE], General Anesthetic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 51662-1542-1

20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)
Marketing Start Date2022-04-09
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "ETOMIDATE" or generic name "Etomidate"

NDCBrand NameGeneric Name
0143-9310EtomidateEtomidate
0143-9311EtomidateEtomidate
0143-9506EtomidateEtomidate
0143-9507EtomidateEtomidate
23155-160EtomidateEtomidate
23155-522EtomidateEtomidate
25021-674etomidateetomidate
51662-1485ETOMIDATEETOMIDATE
51662-1542ETOMIDATEETOMIDATE
55150-221ETOMIDATEETOMIDATE
55150-222ETOMIDATEETOMIDATE
65145-127EtomidateEtomidate
65145-128EtomidateEtomidate
65219-445EtomidateEtomidate
65219-447EtomidateEtomidate
65841-818etomidateetomidate
67457-902EtomidateEtomidate
67457-903EtomidateEtomidate
68083-234EtomidateEtomidate Injection
68083-235EtomidateEtomidate Injection
68382-545etomidateetomidate
70518-1003EtomidateEtomidate
70860-652EtomidateEtomidate
72266-146EtomidateEtomidate
72266-147EtomidateEtomidate
0404-9811AmidateEtomidate
0409-6695AmidateETOMIDATE
0409-8060AmidateEtomidate
52584-695AmidateEtomidate

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.