52652-8001 : Zonisade 100 mg/5ml Oral Suspension
NDC: | 52652-8001 |
Labeler: | Azurity Phramaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Zonisade |
Dosage Form: | Oral Suspension |
Application #: | NDA214273 |
Rev. Date: |
NDC Package Codes:
- 52652-8001-1: 1 BOTTLE IN 1 CARTON (52652‑8001‑1) > 150 ML IN 1 BOTTLE
Active Ingredients:
- Zonisamide
Dosage Strength:
- 100 mg/5mL
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Carbonic Anhydrase Inhibitors [MoA]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
- P-Glycoprotein Inhibitors [MoA]
- Sulfonamides [CS]
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.