NDC 54868-4249 Terazosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
PINK (C48328)
TURQUOISE (C48334)
GG622
GG623
GG624
Code Structure Chart
Product Details
What is NDC 54868-4249?
What are the uses for Terazosin Hydrochloride?
Which are Terazosin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- TERAZOSIN HYDROCHLORIDE (UNII: D32S14F082)
- TERAZOSIN (UNII: 8L5014XET7) (Active Moiety)
Which are Terazosin 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)
- CROSPOVIDONE (UNII: 68401960MK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SHELLAC (UNII: 46N107B71O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
What is the NDC to RxNorm Crosswalk for Terazosin Hydrochloride?
- RxCUI: 260376 - terazosin HCl 10 MG Oral Capsule
- RxCUI: 260376 - terazosin 10 MG Oral Capsule
- RxCUI: 260376 - terazosin (as terazosin HCl) 10 MG Oral Capsule
- RxCUI: 313215 - terazosin HCl 1 MG Oral Capsule
- RxCUI: 313215 - terazosin 1 MG 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".