81864-101 : Ojjaara 200 mg Oral Tablet


NDC: 81864-101
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Ojjaara
Dosage Form: Oral Tablet
Application #: NDA216873
Rev. Date: 


NDC Package Codes:

  • 81864-101-30: 30 TABLET IN 1 BOTTLE (81864‑101‑30)

Active Ingredients:

  • Momelotinib Dihydrochloride Monohydrate

Dosage Strength:

  • 200 mg

Related Products:

Based on records with the same trade name.
  • 81864-102 Ojjaara 150 mg Oral Tablet by Glaxosmithkline LLC
  • 81864-103 Ojjaara 100 mg Oral Tablet by Glaxosmithkline LLC

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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.