|Product Type:||Human Prescription Drug|
|Drug Name:||Levetiracetam Extended-release|
|Dosage Form:||Oral Tablet, Film Coated, Extended Release|
NDC Package Codes:
- 52817-110-32: 300 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (52817‑110‑32)
- 52817-110-60: 60 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE, PLASTIC (52817‑110‑60)
- 500 mg
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
Related Products:Based on records with the same trade name.
- 52817-111 Levetiracetam Extended-release 750 mg Oral Tablet, Film Coated, Extended Release by Trupharma, LLC
- 29033-042 Levetiracetam Extended-release Extended-release 500 mg Oral Tablet, Extended Release by Nostrum Laboratories, Inc.
- 29033-043 Levetiracetam Extended-release Extended-release 750 mg Oral Tablet, Extended Release by Nostrum Laboratories, Inc.
- 35208-031 Levetiracetam Extended-release 500 mg Oral Tablet, Extended Release by Intellipharmaceutics Corp.
- 35208-032 Levetiracetam Extended-release 750 mg Oral Tablet, Extended Release by Intellipharmaceutics Corp.
- 40051-079 Levetiracetam Extended-release Extended-release 750 mg Oral Tablet by Lotus Pharmaceutical Co., Ltd. Nantou Plant
- 40051-332 Levetiracetam Extended-release Extended-release 500 mg Oral Tablet by Lotus Pharmaceutical Co., Ltd. Nantou Plant
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Notice: The MedsChat® 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.