NDC 54868-6159 Pramipexole Dihydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6159 - Pramipexole Dihydrochloride
Product Characteristics
ROUND (C48348)
9 MM
8 MM
B;C;5
B;C;3
Product Packages
NDC Code 54868-6159-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-6159-1
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-6159?
What are the uses for Pramipexole Dihydrochloride?
Which are Pramipexole Dihydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMIPEXOLE DIHYDROCHLORIDE (UNII: 3D867NP06J)
- PRAMIPEXOLE (UNII: 83619PEU5T) (Active Moiety)
Which are Pramipexole Dihydrochloride 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- MANNITOL (UNII: 3OWL53L36A)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Pramipexole Dihydrochloride?
- RxCUI: 859033 - pramipexole dihydrochloride 0.125 MG Oral Tablet
- RxCUI: 859033 - pramipexole dihydrochloride 0.125 MG (pramipexole 0.088 MG) Oral Tablet
- RxCUI: 859040 - pramipexole dihydrochloride 0.25 MG Oral Tablet
- RxCUI: 859040 - pramipexole dihydrochloride 0.25 MG (pramipexole 0.18 MG) Oral Tablet
- RxCUI: 859044 - pramipexole dihydrochloride 0.5 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".