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70518-1191 NDC - TERBINAFINE ()

Drug Information

Product NDC: 70518-1191

Proprietary Name: Terbinafine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: REMEDYREPACK INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/14/2018

Package Information

No. Package Code Package Description Billing Unit
170518-1191-030 TABLET in 1 BOTTLE, PLASTIC (70518-1191-0)
270518-1191-130 TABLET in 1 BLISTER PACK (70518-1191-1)
370518-1191-230 TABLET in 1 BLISTER PACK (70518-1191-2)
470518-1191-345 TABLET in 1 BOTTLE, PLASTIC (70518-1191-3)
570518-1191-490 TABLET in 1 BOTTLE, PLASTIC (70518-1191-4)
670518-1191-514 TABLET in 1 BOTTLE, PLASTIC (70518-1191-5)
770518-1191-660 TABLET in 1 BOTTLE, PLASTIC (70518-1191-6)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70518-1191The 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 NAMETerbinafineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/14/2018This 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: 5/3/2024
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