NDC 0143-9392

REMIFENTANIL HYDROCHLORIDE

Remifentanil Hydrochloride

REMIFENTANIL HYDROCHLORIDE is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Hikma Pharmaceuticals Usa Inc.. The primary component is Remifentanil Hydrochloride.

Product ID0143-9392_0bc4c167-59ce-43ad-9db8-281e4a166887
NDC0143-9392
Product TypeHuman Prescription Drug
Proprietary NameREMIFENTANIL HYDROCHLORIDE
Generic NameRemifentanil Hydrochloride
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2021-05-15
Marketing CategoryANDA /
Application NumberANDA210594
Labeler NameHikma Pharmaceuticals USA Inc.
Substance NameREMIFENTANIL HYDROCHLORIDE
Active Ingredient Strength2 mg/2mL
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0143-9392-10

10 VIAL in 1 CARTON (0143-9392-10) > 5 mL in 1 VIAL (0143-9392-01)
Marketing Start Date2021-05-15
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "REMIFENTANIL HYDROCHLORIDE" or generic name "Remifentanil Hydrochloride"

NDCBrand NameGeneric Name
0143-9391REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
0143-9392REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
0143-9393REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
63323-723Remifentanil HydrochlorideRemifentanil Hydrochloride
63323-724Remifentanil HydrochlorideRemifentanil Hydrochloride
63323-725Remifentanil HydrochlorideRemifentanil Hydrochloride
68475-505REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
68475-506REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
68475-507REMIFENTANIL HYDROCHLORIDEREMIFENTANIL HYDROCHLORIDE
67457-198UltivaRemifentanil Hydrochloride
67457-912UltivaRemifentanil Hydrochloride
67457-913UltivaRemifentanil Hydrochloride
67457-914UltivaRemifentanil Hydrochloride

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