NDC 68071-5118 Tamsulosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-5118 - Tamsulosin Hydrochloride
Product Characteristics
ORANGE (C48331 - ORANGE OPAQUE)
Product Packages
NDC Code 68071-5118-1
Package Description: 100 CAPSULE in 1 BOTTLE
Product Details
What is NDC 68071-5118?
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)
- MICROCRYSTALLINE CELLULOSE (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
* Please review the disclaimer below.
Patient Education
Tamsulosin
Tamsulosin is used in men to treat the symptoms of an enlarged prostate (benign prostatic hyperplasia or BPH) which include difficulty urinating (hesitation, dribbling, weak stream, and incomplete bladder emptying), painful urination, and urinary frequency and urgency. Tamsulosin is in a class of medications called alpha blockers. It works by relaxing the muscles in the prostate and bladder so that urine can flow easily.
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* Please review the disclaimer below.
[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".