51655-092 NDC - LEVOTHYROXINE SODIUM ()

Drug Information

Field Name	Field Value
Labeler Name:	Northwind Pharmaceuticals, LLC
Product Type:
FDA Application Number:	NDA021210
Marketing Category:	NDA
Start Marketing Date:	7/31/2014

No.	Package Code	Package Description	Billing Unit
1	51655-092-52	30 TABLET in 1 BOTTLE, DISPENSING (51655-092-52)

Field Name	Field Value	Definition
PRODUCT NDC	51655-092	The 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 NAME	Levothyroxine Sodium	The 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.
START MARKETING DATE	7/31/2014	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	NDA	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
APPLICATION NUMBER	NDA021210	The translation of the dosage form Code submitted by the firm.
LABELER NAME	Northwind Pharmaceuticals, LLC	This is the date that the labeler indicates was the start of its marketing of the drug product.