57297-351 NDC - SERTRALINE ()

Drug Information

Product NDC: 57297-351

Proprietary Name: Sertraline

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: LUPIN LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/6/2007

Package Information

No. Package Code Package Description Billing Unit
157297-351-01100 TABLET, FILM COATED in 1 BOTTLE (57297-351-01)
257297-351-031000 TABLET, FILM COATED in 1 BOTTLE (57297-351-03)
357297-351-0630 TABLET, FILM COATED in 1 BOTTLE (57297-351-06)
457297-351-0850 TABLET, FILM COATED in 1 BOTTLE (57297-351-08)
557297-351-0990 TABLET, FILM COATED in 1 BOTTLE (57297-351-09)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57297-351The 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 NAMESertralineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/6/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELUPIN LIMITEDName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023