70518-0513 NDC - LAMIVUDINE ()

Drug Information

Product NDC: 70518-0513

Proprietary Name: Lamivudine

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/9/2017

Package Information

No. Package Code Package Description Billing Unit
170518-0513-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0513-0)
270518-0513-18 TABLET, FILM COATED in 1 BLISTER PACK (70518-0513-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70518-0513The 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 NAMELamivudineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/9/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEREMEDYREPACK INC.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/21/2020