65727-068 NDC - SIMVASTATIN ()

Drug Information

Product NDC: 65727-068

Proprietary Name: Simvastatin

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Biocon Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/17/2015

Package Information

No. Package Code Package Description Billing Unit
165727-068-1230 TABLET, FILM COATED in 1 BOTTLE (65727-068-12)
265727-068-1345 TABLET, FILM COATED in 1 BOTTLE (65727-068-13)
365727-068-1490 TABLET, FILM COATED in 1 BOTTLE (65727-068-14)
465727-068-151000 TABLET, FILM COATED in 1 BOTTLE (65727-068-15)

NDC Record

Field Name Field Value Definition
PRODUCT NDC65727-068The 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 NAMESimvastatinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/17/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBiocon LimitedName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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