Zelboraf - Vemurafenib 240 mg / 1 Tablet 1 Bottle, Plastic

Reference details for licensed healthcare facility review and verification.

Vemurafenib NDC Family 50242-0090 Vemurafenib 240 mg / 1

NDC 11	50242-0090-02
Product NDC	50242-0090
Generic Drug Name	Vemurafenib
Brand Name	Zelboraf
Manufacturer	Genentech, Inc.
Strength	240 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	1 Bottle, Plastic
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (50242-090-02) / 112 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Active Ingredients	Vemurafenib
Marketing Category	NDA

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NDC snapshot

Vemurafenib 240 mg / 1 Tablet is tracked under NDC 50242-0090-02 and rolls up into product family 50242-0090. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 1 Bottle, Plastic.
Manufacturer: Genentech, Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Official references

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Zelboraf - Vemurafenib 240 mg / 1 Tablet 1 Bottle, Plastic, NDC 50242-0090-02, is a Genentech, Inc. 240 mg / 1 tablet presentation packaged as 1 Bottle, Plastic.

NDC search formats

Canonical NDC 11: 50242-0090-02
Digits-only NDC 11: 50242009002
Possible 10-digit display formats: 50242-090-02 (5024209002), 50242-0090-2 (5024200902)

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: Zelboraf
NDC 11: 50242-0090-02
Product family NDC: 50242-0090
VA classification code: AN900
VA classification code description: ANTINEOPLASTIC,OTHER
CMOP ID: V0218
VUID: 4030953