NDC 54868-3714 Timolol Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3714 - Timolol Maleate
Product Packages
NDC Code 54868-3714-1
Package Description: 10 mL in 1 BOTTLE, PLASTIC
NDC Code 54868-3714-2
Package Description: 5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3714?
What are the uses for Timolol Maleate?
Which are Timolol Maleate UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIMOLOL MALEATE (UNII: P8Y54F701R)
- TIMOLOL ANHYDROUS (UNII: 5JKY92S7BR) (Active Moiety)
Which are Timolol Maleate 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Timolol Maleate?
- RxCUI: 1923428 - timolol maleate 0.25 % Ophthalmic Solution
- RxCUI: 1923428 - timolol 2.5 MG/ML Ophthalmic Solution
- RxCUI: 1923428 - timolol 0.25 % Ophthalmic Solution
- RxCUI: 1923428 - timolol 2.5 MG/ML (as timolol maleate 3.4 MG/ML) Ophthalmic Solution
- RxCUI: 1992303 - timolol 0.5 % 12HR Ophthalmic Solution
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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".