70518-3010 : Latuda 80 mg Oral Tablet, Film Coated


NDC70518-3010
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Latuda
Dosage Form: Oral Tablet, Film Coated
Application #: NDA200603
Rev. Date: 


NDC Package Codes:

  • 70518-3010-0: 30 POUCH IN 1 BOX (70518‑3010‑0) > 1 TABLET, FILM COATED IN 1 POUCH (70518‑3010‑1)

Active Ingredients:

  • Lurasidone Hydrochloride

Dosage Strength:

  • 80 mg

Pharmaceutical Classes:

  • Atypical Antipsychotic [EPC]

Related Products:

Based on records with the same trade name.
  • 70518-1812 Latuda 60 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1824 Latuda 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-1936 Latuda 120 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 51148-001 Latuda 40 mg Oral Tablet by Bushu Pharmaceutical, Ltd.
  • 51148-002 Latuda 80 mg Oral Tablet by Bushu Pharmaceutical, Ltd.
  • 63402-302 Latuda 20 mg Oral Tablet by Sunovion Pharmaceuticals Inc.
  • 63402-304 Latuda 40 mg Oral Tablet by Sunovion Pharmaceuticals Inc.
  • 63402-306 Latuda 60 mg Oral Tablet by Sunovion Pharmaceuticals Inc.
  • 63402-308 Latuda 80 mg Oral Tablet by Sunovion Pharmaceuticals Inc.
  • 63402-312 Latuda 120 mg Oral Tablet by Sunovion Pharmaceuticals Inc.
  • 69189-0316 Latuda 40 mg Oral Tablet, Film Coated by Avera Mckennan Hospital

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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.