NDC 80175-0582 Duloxetine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80175 - Central Packaging
- 80175-0582 - Duloxetine
Product Characteristics
WHITE (C48325)
Product Packages
NDC Code 80175-0582-3
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 80175-0582?
What are the uses for Duloxetine?
Which are Duloxetine UNII Codes?
The UNII codes for the active ingredients in this product are:
- DULOXETINE HYDROCHLORIDE (UNII: 9044SC542W)
- DULOXETINE (UNII: O5TNM5N07U) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Duloxetine?
- 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
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[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".