NDC 42254-096 Lorazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42254 - Rebel Distributors Corp
- 42254-096 - Lorazepam
Product Characteristics
7 MM
EP;905
Product Packages
NDC Code 42254-096-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 42254-096-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 42254-096-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 42254-096-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 42254-096?
What are the uses for Lorazepam?
Which are Lorazepam UNII Codes?
The UNII codes for the active ingredients in this product are:
- LORAZEPAM (UNII: O26FZP769L)
- LORAZEPAM (UNII: O26FZP769L) (Active Moiety)
Which are Lorazepam 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Lorazepam?
- RxCUI: 197900 - LORazepam 0.5 MG Oral Tablet
- RxCUI: 197900 - lorazepam 0.5 MG Oral Tablet
- RxCUI: 197901 - LORazepam 1 MG Oral Tablet
- RxCUI: 197901 - lorazepam 1 MG Oral Tablet
- RxCUI: 197902 - LORazepam 2 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".