65841-776 NDC - DULOXETINE ()

Drug Information

Product NDC: 65841-776

Proprietary Name: Duloxetine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Cadila Healthcare Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/15/2014

Package Information

No. Package Code Package Description Billing Unit
165841-776-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-776-06)
265841-776-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-776-10)
365841-776-1690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-776-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC65841-776The 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 NAMEDuloxetineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/15/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECadila Healthcare 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