NDC 21695-146 Cymbalta

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21695-146
Proprietary Name:
Cymbalta
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp.
Labeler Code:
21695
Start Marketing Date: [9]
08-24-2004
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - OPAQUE BLUE)
WHITE (C48325 - OPAQUE WHITE)
GREEN (C48329 - OPAQUE GREEN)
Shape:
CAPSULE (C48336)
Size(s):
16 MM
20 MM
Imprint(s):
LILLY;3240;30;MG
LILLY;3237;60;MG
Score:
1

Product Packages

NDC Code 21695-146-15

Package Description: 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Code 21695-146-30

Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Product Details

What is NDC 21695-146?

The NDC code 21695-146 is assigned by the FDA to the product Cymbalta which is product labeled by Rebel Distributors Corp.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 21695-146-15 15 capsule, delayed release in 1 bottle , 21695-146-30 30 capsule, delayed release in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Cymbalta?

Duloxetine is used to treat depression and anxiety. In addition, duloxetine is used to help relieve nerve pain (peripheral neuropathy) in people with diabetes or ongoing pain due to medical conditions such as arthritis, chronic back pain, or fibromyalgia (a condition that causes widespread pain). Duloxetine may improve your mood, sleep, appetite, and energy level, and decrease nervousness. It can also decrease pain due to certain medical conditions. Duloxetine is known as a serotonin-norepinephrine reuptake inhibitor (SNRI). This medication works by helping to restore the balance of certain natural substances (serotonin and norepinephrine) in the brain.

Which are Cymbalta UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Cymbalta Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Cymbalta?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 596930 - DULoxetine 30 MG Delayed Release Oral Capsule
  • RxCUI: 596930 - duloxetine 30 MG Delayed Release Oral Capsule
  • RxCUI: 596930 - duloxetine 30 MG (as duloxetine HCl 33.7 MG) Delayed Release Oral Capsule
  • RxCUI: 596932 - Cymbalta 30 MG Delayed Release Oral Capsule
  • RxCUI: 596932 - duloxetine 30 MG Delayed Release Oral Capsule [Cymbalta]

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".