NDC 50436-2996 Duloxetine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325 - OPAQUE WHITE)
BLUE (C48333 - OPAQUE BLUE)
16 MM
APO;D30
Code Structure Chart
Product Details
What is NDC 50436-2996?
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:
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- METHYLCELLULOSE (15 MPA.S) (UNII: NPU9M2E6L8)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- TALC (UNII: 7SEV7J4R1U)
- POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- SHELLAC (UNII: 46N107B71O)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- AMMONIA (UNII: 5138Q19F1X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
What is the NDC to RxNorm Crosswalk for Duloxetine Hydrochloride?
- 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.
[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".