NDC 53145-057 Threda
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53145 - Menper Distributors, Inc.
- 53145-057 - Threda
Product Packages
NDC Code 53145-057-04
Package Description: 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE
Product Details
What is NDC 53145-057?
Which are Threda UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Threda 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)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- D&C RED NO. 22 (UNII: 1678RKX8RT)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SORBIC ACID (UNII: X045WJ989B)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Threda?
- RxCUI: 1437923 - THREDA 262 MG in 15 mL Oral Suspension
- RxCUI: 1437923 - bismuth subsalicylate 17.5 MG/ML Oral Suspension [Threda]
- RxCUI: 1437923 - Threda 17.5 MG/ML Oral Suspension
- RxCUI: 1437923 - Threda 262 MG per 15 ML Oral Suspension
- RxCUI: 308762 - bismuth subsalicylate 525 MG in 30 mL Oral Suspension
* 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".