NDC 53808-0586 Sertraline Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0586 - Sertraline Hydrochloride
Product Characteristics
Product Packages
NDC Code 53808-0586-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 53808-0586?
Which are Sertraline Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- SERTRALINE HYDROCHLORIDE (UNII: UTI8907Y6X)
- SERTRALINE (UNII: QUC7NX6WMB) (Active Moiety)
Which are Sertraline 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:
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Sertraline Hydrochloride?
- RxCUI: 312940 - sertraline HCl 25 MG Oral Tablet
- RxCUI: 312940 - sertraline 25 MG Oral Tablet
- RxCUI: 312940 - sertraline (as sertraline HCl) 25 MG Oral Tablet
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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".