NDC 64725-0507 Citalopram Hydrobromide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0507 - Citalopram Hydrobromide
Product Characteristics
Product Packages
NDC Code 64725-0507-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 64725-0507?
What are the uses for Citalopram Hydrobromide?
Which are Citalopram Hydrobromide UNII Codes?
The UNII codes for the active ingredients in this product are:
- CITALOPRAM HYDROBROMIDE (UNII: I1E9D14F36)
- CITALOPRAM (UNII: 0DHU5B8D6V) (Active Moiety)
Which are Citalopram Hydrobromide 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Citalopram Hydrobromide?
- RxCUI: 283672 - citalopram 10 MG Oral Tablet
- RxCUI: 283672 - citalopram 10 MG (as citalopram HBr 12.49 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".