NDC 53808-0988 Fluoxetine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0988 - Fluoxetine Hydrochloride
Product Characteristics
Product Packages
NDC Code 53808-0988-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0988?
What are the uses for Fluoxetine Hydrochloride?
Which are Fluoxetine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLUOXETINE HYDROCHLORIDE (UNII: I9W7N6B1KJ)
- FLUOXETINE (UNII: 01K63SUP8D) (Active Moiety)
Which are Fluoxetine 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Fluoxetine Hydrochloride?
- RxCUI: 313990 - FLUoxetine HCl 10 MG Oral Tablet
- RxCUI: 313990 - fluoxetine 10 MG Oral Tablet
- RxCUI: 313990 - fluoxetine 10 MG (as fluoxetine hydrochloride 11.2 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".