NDC 54868-4437 Tamsulosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329 - LIGHT GREEN OPAQUE)
Code Structure Chart
Product Details
What is NDC 54868-4437?
What are the uses for Tamsulosin Hydrochloride?
Which are Tamsulosin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- TAMSULOSIN HYDROCHLORIDE (UNII: 11SV1951MR)
- TAMSULOSIN (UNII: G3P28OML5I) (Active Moiety)
Which are Tamsulosin 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:
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- COPOVIDONE (UNII: D9C330MD8B)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
What is the NDC to RxNorm Crosswalk for Tamsulosin Hydrochloride?
- RxCUI: 863669 - tamsulosin HCl 0.4 MG Oral Capsule
- RxCUI: 863669 - tamsulosin hydrochloride 0.4 MG Oral Capsule
- RxCUI: 863669 - tamsulosin HCl 0.4 MG Modified Release Oral Capsule
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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".