NDC 64725-1100 Duloxetine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-1100 - Duloxetine Hydrochloride
Product Characteristics
Product Packages
NDC Code 64725-1100-1
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 64725-1100?
What are the uses for Duloxetine Hydrochloride?
Which are Duloxetine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- DULOXETINE HYDROCHLORIDE (UNII: 9044SC542W)
- DULOXETINE (UNII: O5TNM5N07U) (Active Moiety)
Which are Duloxetine Hydrochloride 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Duloxetine Hydrochloride?
- 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".