Ojjaara - Momelotinib 200 mg / 1 Tablet 30 Tablet

Reference details for licensed healthcare facility review and verification.

Momelotinib NDC Family 81864-0101 Momelotinib 200 mg / 1

NDC 11	81864-0101-30
Product NDC	81864-0101
Generic Drug Name	Momelotinib
Brand Name	Ojjaara
Manufacturer	GlaxoSmithKline LLC
Strength	200 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet
Package Description	30 TABLET in 1 BOTTLE (81864-101-30)
Active Ingredients	Momelotinib Dihydrochloride Monohydrate
Marketing Category	NDA

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NDC snapshot

Momelotinib 200 mg / 1 Tablet is tracked under NDC 81864-0101-30 and rolls up into product family 81864-0101. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 30 Tablet.
Manufacturer: GlaxoSmithKline LLC.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Official references

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Ojjaara - Momelotinib 200 mg / 1 Tablet 30 Tablet, NDC 81864-0101-30, is a GlaxoSmithKline LLC 200 mg / 1 tablet presentation packaged as 30 Tablet.

NDC search formats

Canonical NDC 11: 81864-0101-30
Digits-only NDC 11: 81864010130
Possible 10-digit display format: 81864-101-30 (8186410130)

Helpful product links

Search by brand name: Ojjaara
Exact NDC 11: 81864-0101-30
Product family NDC: 81864-0101
VA classification code: AN900
VA classification code description: ANTINEOPLASTIC,OTHER
CMOP ID: M1328
VUID: 4042620