15631-0620 NDC - LACHESIS MUTUS ()

Drug Information

Product NDC: 15631-0620

Proprietary Name: LACHESIS MUTUS

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/24/2015

Package Information

No. Package Code Package Description Billing Unit
115631-0620-01 TABLET in 1 BLISTER PACK (15631-0620-0)
215631-0620-14 TABLET in 1 BLISTER PACK (15631-0620-1)
315631-0620-250 TABLET in 1 CONTAINER (15631-0620-2)
415631-0620-3100 TABLET in 1 CONTAINER (15631-0620-3)
515631-0620-4250 TABLET in 1 CONTAINER (15631-0620-4)
615631-0620-5500 TABLET in 1 CONTAINER (15631-0620-5)
715631-0620-61000 TABLET in 1 CONTAINER (15631-0620-6)
815631-0620-710000 TABLET in 1 CONTAINER (15631-0620-7)

NDC Record

Field Name Field Value Definition
PRODUCT NDC15631-0620The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMELACHESIS MUTUSThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/24/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERxhomeo Private Limited d.b.a. Rxhomeo, IncName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 10/4/2019