Trintellix - Vortioxetine 20 mg / 1 Tablet 2430 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

vortioxetine NDC Family 55154-0257 vortioxetine 20 mg / 1

NDC 11	55154-0257-08
Product NDC	55154-0257
Generic Drug Name	vortioxetine
Brand Name	Trintellix
Manufacturer	Cardinal Health 107, LLC
Strength	20 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	2430 Tablet, Film Coated
Package Description	2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)
Active Ingredients	Vortioxetine Hydrobromide
Marketing Category	NDA

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NDC snapshot

vortioxetine 20 mg / 1 Tablet is tracked under NDC 55154-0257-08 and rolls up into product family 55154-0257. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 2430 Tablet, Film Coated.
Manufacturer: Cardinal Health 107, LLC.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyvortioxetine

Official references

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Trintellix - Vortioxetine 20 mg / 1 Tablet 2430 Tablet, Film Coated, NDC 55154-0257-08, is a Cardinal Health 107, LLC 20 mg / 1 tablet presentation packaged as 2430 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 55154-0257-08
Digits-only NDC 11: 55154025708
Possible 10-digit display formats: 55154-257-08 (5515425708), 55154-0257-8 (5515402578)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

Helpful product links

Search by brand name: Trintellix
Exact NDC 11: 55154-0257-08
Product family NDC: 55154-0257
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: V0249
VUID: 4032790