NDC 68151-3645 Pramipexole Dihydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-3645 - Pramipexole Dihydrochloride
Product Characteristics
Product Packages
NDC Code 68151-3645-9
Package Description: 1 TABLET in 1 PACKAGE
Product Details
What is NDC 68151-3645?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- POVIDONE K30 (UNII: U725QWY32X)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Pramipexole Dihydrochloride?
- RxCUI: 859052 - pramipexole dihydrochloride 1 MG Oral Tablet
- RxCUI: 859052 - pramipexole dihydrochloride 1 MG (pramipexole 0.7 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".