NDC 81864-101 – Ojjaara

Momelotinib Dihydrochloride Monohydrate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC81864-101

Product details

Brand name
Ojjaara
Generic name
Momelotinib
Labeler
GlaxoSmithKline LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA216873
Marketed since
September 15, 2023
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ojjaara →

Package NDC codes (1)

Package NDCDescriptionSince
81864-101-3030 TABLET in 1 BOTTLE (81864-101-30)Sep 15, 2023

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