NDC 0404-9880

KETALAR

Ketamine Hydrochloride

KETALAR is a Intramuscular; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Henry Schein, Inc. The primary component is Ketamine Hydrochloride.

Product ID0404-9880_5eee5a1d-c99a-41c4-9966-a4c3ce0a287f
NDC0404-9880
Product TypeHuman Prescription Drug
Proprietary NameKETALAR
Generic NameKetamine Hydrochloride
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2022-01-11
Marketing CategoryNDA /
Application NumberNDA016812
Labeler NameHenry Schein, Inc
Substance NameKETAMINE HYDROCHLORIDE
Active Ingredient Strength10 mg/mL
Pharm ClassesGeneral Anesthesia [PE],General Anesthetic [EPC]
DEA ScheduleCIII
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0404-9880-20

1 VIAL in 1 BAG (0404-9880-20) > 20 mL in 1 VIAL
Marketing Start Date2022-01-11
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "KETALAR" or generic name "Ketamine Hydrochloride"

NDCBrand NameGeneric Name
0404-9880KETALARketamine hydrochloride
42023-113Ketalarketamine hydrochloride
42023-114Ketalarketamine hydrochloride
42023-115Ketalarketamine hydrochloride
52584-037KETALARketamine hydrochloride
0143-9508Ketamine HydrochlorideKetamine Hydrochloride
0143-9509Ketamine HydrochlorideKetamine Hydrochloride
0404-9881KETAMINE HYDROCHLORIDEketamine hydrochloride
0404-9882KETAMINE HYDROCHLORIDEketamine hydrochloride
0409-0040Ketamine HydrochlorideKETAMINE HYDROCHLORIDE
0409-2051Ketamine HydrochlorideKETAMINE HYDROCHLORIDE
0409-2053Ketamine HydrochlorideKETAMINE HYDROCHLORIDE

Trademark Results [KETALAR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KETALAR
KETALAR
72276388 0840783 Live/Registered
PARKE, DAVIS & COMPANY
1967-07-20

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