NDC 69097-297 Duloxetine

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:
69097-297
Proprietary Name:
Duloxetine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cipla Usa Inc.
Labeler Code:
69097
Start Marketing Date: [9]
12-05-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - OPAQUE GREEN)
WHITE (C48325 - CLEAR TRANSPARENT)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Imprint(s):
297;CIPLA
Score:
1

Product Packages

NDC Code 69097-297-02

Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Code 69097-297-03

Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Price per Unit: $0.16258 per EA

NDC Code 69097-297-05

Package Description: 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Code 69097-297-15

Package Description: 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Product Details

What is NDC 69097-297?

The NDC code 69097-297 is assigned by the FDA to the product Duloxetine which is product labeled by Cipla Usa Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 69097-297-02 30 capsule, delayed release in 1 bottle , 69097-297-03 60 capsule, delayed release in 1 bottle , 69097-297-05 90 capsule, delayed release in 1 bottle , 69097-297-15 1000 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.

Which are Duloxetine UNII Codes?

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

Which are Duloxetine 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 Duloxetine?

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: 596926 - DULoxetine 20 MG Delayed Release Oral Capsule
  • RxCUI: 596926 - duloxetine 20 MG Delayed Release Oral Capsule
  • RxCUI: 596926 - duloxetine 20 MG (as duloxetine HCl 22.4 MG) Delayed Release Oral Capsule
  • RxCUI: 596930 - DULoxetine 30 MG Delayed Release Oral Capsule
  • RxCUI: 596930 - duloxetine 30 MG Delayed Release Oral Capsule

* 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".