NDC 64725-1473 Prednisone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-1473 - Prednisone
Product Characteristics
Product Packages
NDC Code 64725-1473-1
Package Description: 30 TABLET in 1 CONTAINER
Product Details
What is NDC 64725-1473?
What are the uses for Prednisone?
Which are Prednisone UNII Codes?
The UNII codes for the active ingredients in this product are:
- PREDNISONE (UNII: VB0R961HZT)
- PREDNISONE (UNII: VB0R961HZT) (Active Moiety)
Which are Prednisone 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Prednisone?
- RxCUI: 198145 - predniSONE 10 MG Oral Tablet
- RxCUI: 198145 - prednisone 10 MG Oral Tablet
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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".