Inluriyo - Imlunestrant 200 mg / 1 Tablet 28 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

imlunestrant NDC Family 00002-1717 imlunestrant 200 mg / 1

NDC 11	00002-1717-28
Product NDC	00002-1717
Generic Drug Name	imlunestrant
Brand Name	Inluriyo
Manufacturer	Eli Lilly and Company
Strength	200 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	28 Tablet, Film Coated
Package Description	28 TABLET, FILM COATED in 1 BOTTLE (0002-1717-28)
Active Ingredients	Imlunestrant
Marketing Category	NDA

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NDC snapshot

imlunestrant 200 mg / 1 Tablet is tracked under NDC 00002-1717-28 and rolls up into product family 00002-1717. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 28 Tablet, Film Coated.
Manufacturer: Eli Lilly and Company.
Dosage form: Tablet.
Family size: 2 indexed presentations.

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Alternate presentations in this family

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Inluriyo - Imlunestrant 200 mg / 1 Tablet 56 Tablet, Film CoatedNDC 00002-1717-56 | 56 Tablet, Film Coated | Eli Lilly and Company

Inluriyo - Imlunestrant 200 mg / 1 Tablet 28 Tablet, Film Coated, NDC 00002-1717-28, is a Eli Lilly and Company 200 mg / 1 tablet presentation packaged as 28 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 00002-1717-28
Digits-only NDC 11: 00002171728
Possible 10-digit display format: 0002-1717-28 (0002171728)

Helpful product links

Search by brand name: Inluriyo
NDC 11: 00002-1717-28
Product family NDC: 00002-1717
Other package sizes in this family: 56 Tablet, Film Coated
Compare related presentations: Inluriyo - Imlunestrant 200 mg / 1 Tablet 56 Tablet, Film Coated
VA classification code: AN500
VA classification code description: ANTINEOPLASTIC HORMONES
CMOP ID: I0803
VUID: 4044297