NDC 67046-721 Tamsulosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ORANGE (C48331 - ORANGE OPAQUE)
Code Structure Chart
Product Details
What is NDC 67046-721?
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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- GELATIN (UNII: 2G86QN327L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TRIACETIN (UNII: XHX3C3X673)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- AMMONIA (UNII: 5138Q19F1X)
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".