59651-367 : Vigabatrin 500 mg Oral Tablet


NDC: 59651-367
Labeler: Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Vigabatrin
Dosage Form: Oral Tablet
Application #: ANDA215601
Rev. Date: 


NDC Package Codes:

  • 59651-367-01: 1 BOTTLE IN 1 CARTON (59651‑367‑01) > 100 TABLET IN 1 BOTTLE

Active Ingredients:

  • Vigabatrin

Dosage Strength:

  • 500 mg

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]

Related Products:

Based on records with the same trade name.
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  • 42799-950 Vigabatrin 500 mg Oral Tablet by Edenbridge Pharmaceuticals LLC.
  • 43598-651 Vigabatrin 500 mg Oral Tablet, Film Coated by Dr. Reddy¿s Laboratories Inc.,
  • 43598-697 Vigabatrin 50 mg/ml Oral Powder, for Solution by Dr. Reddy¿s Laboratories Inc.,
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  • 60219-1425 Vigabatrin 500 mg Oral for Solution by Amneal Pharmaceuticals Ny LLC
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  • 69097-964 Vigabatrin 500 mg/ml Oral Powder, for Solution by Cipla USA, Inc.
  • 69238-1424 Vigabatrin 500 mg Oral Tablet by Amneal Pharmaceuticals Ny LLC
  • 69238-1425 Vigabatrin 500 mg Oral for Solution by Amneal Pharmaceuticals LLC
  • 70377-089 Vigabatrin 500 mg/10ml Oral Powder, for Solution by Biocon Pharma Inc.
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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.