NDC 68071-3312 Escitalopram Oxalate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals, Inc.
- 68071-3312 - Escitalopram Oxalate
Product Characteristics
Product Packages
NDC Code 68071-3312-3
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 68071-3312-8
Package Description: 28 TABLET in 1 BOTTLE
Product Details
What is NDC 68071-3312?
What are the uses for Escitalopram Oxalate?
Which are Escitalopram Oxalate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESCITALOPRAM OXALATE (UNII: 5U85DBW7LO)
- ESCITALOPRAM (UNII: 4O4S742ANY) (Active Moiety)
Which are Escitalopram Oxalate 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Escitalopram Oxalate?
- RxCUI: 351250 - escitalopram oxalate 20 MG Oral Tablet
- RxCUI: 351250 - escitalopram 20 MG Oral Tablet
- RxCUI: 351250 - escitalopram (as escitalopram oxalate) 20 MG 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".