NDC 35208-009 Desvenlafaxine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 35208 - Intellipharmaceutics Corp.
- 35208-009 - Desvenlafaxine
Product Characteristics
Product Packages
NDC Code 35208-009-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 35208-009-14
Package Description: 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 35208-009?
What are the uses for Desvenlafaxine?
Which are Desvenlafaxine UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESVENLAFAXINE SUCCINATE (UNII: ZB22ENF0XR)
- DESVENLAFAXINE (UNII: NG99554ANW) (Active Moiety)
Which are Desvenlafaxine 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:
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
- ETHYLCELLULOSE (100 MPA.S) (UNII: 47MLB0F1MV)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Desvenlafaxine?
- RxCUI: 1874553 - desvenlafaxine succinate 100 MG 24HR Extended Release Oral Tablet
- RxCUI: 1874553 - 24 HR desvenlafaxine succinate 100 MG Extended Release Oral Tablet
- RxCUI: 1874553 - desvenlafaxine 100 MG (as desvenlafaxine succinate 152 MG) 24HR Extended Release Oral Tablet
- RxCUI: 1874559 - desvenlafaxine succinate 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 1874559 - 24 HR desvenlafaxine succinate 50 MG Extended Release Oral Tablet
* 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".