NDC 58177-910 Prednisolone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58177 - Ethex Corporation
- 58177-910 - Prednisolone
Product Characteristics
Product Packages
NDC Code 58177-910-05
Package Description: 240 mL in 1 BOTTLE
NDC Code 58177-910-07
Package Description: 480 mL in 1 BOTTLE
Product Details
What is NDC 58177-910?
What are the uses for Prednisolone?
Which are Prednisolone UNII Codes?
The UNII codes for the active ingredients in this product are:
- PREDNISOLONE (UNII: 9PHQ9Y1OLM)
- PREDNISOLONE (UNII: 9PHQ9Y1OLM) (Active Moiety)
Which are Prednisolone 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:
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ALCOHOL (UNII: 3K9958V90M)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYL MALTOL (UNII: L6Q8K29L05)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCYRRHIZIN, AMMONIATED (UNII: 3VRD35U26C)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SUCROSE (UNII: C151H8M554)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Prednisolone?
- RxCUI: 283077 - prednisoLONE sodium phosphate 15 MG in 5 mL Oral Solution
- RxCUI: 283077 - prednisolone 3 MG/ML Oral Solution
- RxCUI: 283077 - prednisolone 15 MG (as prednisolone sodium phosphate 20.2 MG) per 5 ML Oral Solution
- RxCUI: 283077 - prednisolone 15 MG per 5 ML Oral Solution
* 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".