NDC 33261-212 Terazosin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-212 - Terazosin
Product Characteristics
YELLOW (C48330)
APO;116
Product Packages
NDC Code 33261-212-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-212?
What are the uses for Terazosin?
Which are Terazosin 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 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)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Terazosin?
- 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
* 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".