63629-7015 NDC - OMEGA-3-ACID ETHYL ESTERS ()

Drug Information

Product NDC: 63629-7015

Proprietary Name: Omega-3-acid ethyl esters

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number: ANDA090973
Marketing Category: ANDA
Start Marketing Date:9/30/2014

Package Information

No. Package Code Package Description Billing Unit
163629-7015-190 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-1)
263629-7015-228 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-2)
363629-7015-360 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-3)
463629-7015-4120 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-4)EA
563629-7015-5100 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-5)
663629-7015-630 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7015-6)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63629-7015The 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 NAMEOmega-3-acid ethyl estersThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA090973This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 6/7/2024