NDC 52652-8001

ZONISADE

Zonisamide

ZONISADE is a Oral Suspension in the Human Prescription Drug category. It is labeled and distributed by Azurity Phramaceuticals, Inc.. The primary component is Zonisamide.

Product ID52652-8001_6db53d1f-51d3-4052-b6d9-1ef1e7431415
NDC52652-8001
Product TypeHuman Prescription Drug
Proprietary NameZONISADE
Generic NameZonisamide
Dosage FormSuspension
Route of AdministrationORAL
Marketing Start Date2022-07-15
Marketing CategoryNDA /
Application NumberNDA214273
Labeler NameAzurity Phramaceuticals, Inc.
Substance NameZONISAMIDE
Active Ingredient Strength100 mg/5mL
Pharm ClassesAnti-epileptic Agent [EPC], Carbonic Anhydrase Inhibitors [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], P-Glycoprotein Inhibitors [MoA], Sulfonamides [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 52652-8001-1

1 BOTTLE in 1 CARTON (52652-8001-1) > 150 mL in 1 BOTTLE
Marketing Start Date2022-07-15
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "ZONISADE" or generic name "Zonisamide"

NDCBrand NameGeneric Name
0185-0193ZonisamideZonisamide
0185-0199ZonisamideZonisamide
0185-0200ZonisamideZonisamide
0378-6725Zonisamidezonisamide
0378-6726Zonisamidezonisamide
0378-6727Zonisamidezonisamide
0615-1379Zonisamidezonisamide
0615-8266zonisamidezonisamide
21695-155ZONISAMIDEZONISAMIDE
21695-654ZONISAMIDEZONISAMIDE
29300-428ZonisamideZonisamide
29300-429ZonisamideZonisamide
29300-430ZonisamideZonisamide
31722-228ZonisamideZonisamide
33261-843ZONISAMIDEZONISAMIDE
35356-143ZONISAMIDEZONISAMIDE
43063-575Zonisamidezonisamide
43063-932ZonisamideZonisamide
50090-2174ZonisamideZonisamide
50268-816ZonisamideZonisamide
51079-768Zonisamidezonisamide
51407-137ZonisamideZonisamide
51407-138ZonisamideZonisamide

Trademark Results [ZONISADE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ZONISADE
ZONISADE
90400843 not registered Live/Pending
Eton Pharmaceuticals, Inc.
2020-12-22

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