NDC 54868-0076 Allopurinol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0076 - Allopurinol
Product Characteristics
ORANGE (C48331)
11 MM
DAN;DAN;5544
Product Packages
NDC Code 54868-0076-2
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 54868-0076-3
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 54868-0076-6
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 54868-0076-7
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 54868-0076-8
Package Description: 180 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-0076?
What are the uses for Allopurinol?
Which are Allopurinol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLOPURINOL (UNII: 63CZ7GJN5I)
- ALLOPURINOL (UNII: 63CZ7GJN5I) (Active Moiety)
Which are Allopurinol 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Allopurinol?
- RxCUI: 197319 - allopurinol 100 MG Oral Tablet
- RxCUI: 197320 - allopurinol 300 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".