NDC 54868-2932 Pristiq Extended-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2932 - Pristiq
Product Characteristics
Product Packages
NDC Code 54868-2932-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-2932?
What are the uses for Pristiq Extended-release?
Which are Pristiq Extended-release UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESVENLAFAXINE SUCCINATE (UNII: ZB22ENF0XR)
- DESVENLAFAXINE (UNII: NG99554ANW) (Active Moiety)
Which are Pristiq Extended-release 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
What is the NDC to RxNorm Crosswalk for Pristiq Extended-release?
- RxCUI: 1874559 - desvenlafaxine succinate 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 1874559 - 24 HR desvenlafaxine succinate 50 MG Extended Release Oral Tablet
- RxCUI: 1874559 - desvenlafaxine 50 MG (as desvenlafaxine succinate 76 MG) 24HR Extended Release Oral Tablet
- RxCUI: 790290 - Pristiq 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 790290 - 24 HR desvenlafaxine succinate 50 MG Extended Release Oral Tablet [Pristiq]
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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".