NDC 33261-594 Alprazolam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 33261-594-00
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-02
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-42
Package Description: 42 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-45
Package Description: 45 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-594-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-594?
What are the uses for Alprazolam?
Which are Alprazolam UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALPRAZOLAM (UNII: YU55MQ3IZY)
- ALPRAZOLAM (UNII: YU55MQ3IZY) (Active Moiety)
Which are Alprazolam 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:
- CROSPOVIDONE (UNII: 68401960MK)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Alprazolam?
- RxCUI: 197321 - ALPRAZolam 1 MG Oral Tablet
- RxCUI: 197321 - alprazolam 1 MG Oral Tablet
- RxCUI: 197322 - ALPRAZolam 2 MG Oral Tablet
- RxCUI: 197322 - alprazolam 2 MG Oral Tablet
- RxCUI: 308047 - ALPRAZolam 0.25 MG Oral Tablet
* 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".