NDC 54868-5667 Bromocriptine Mesylate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5667 - Bromocriptine Mesylate
Product Characteristics
Product Packages
NDC Code 54868-5667-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5667-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5667-2
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5667-3
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5667?
What are the uses for Bromocriptine Mesylate?
Which are Bromocriptine Mesylate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BROMOCRIPTINE MESYLATE (UNII: FFP983J3OD)
- BROMOCRIPTINE (UNII: 3A64E3G5ZO) (Active Moiety)
Which are Bromocriptine Mesylate 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)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALEIC ACID (UNII: 91XW058U2C)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Bromocriptine Mesylate?
- RxCUI: 197411 - bromocriptine mesylate 2.5 MG Oral Tablet
- RxCUI: 197411 - bromocriptine 2.5 MG Oral Tablet
- RxCUI: 197411 - bromocriptine (as bromocriptine mesylate) 2.5 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".