NDC 43353-920 Ropinirole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-920 - Ropinirole
Product Characteristics
Product Packages
NDC Code 43353-920-09
Package Description: 9000 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-920?
What are the uses for Ropinirole?
Which are Ropinirole UNII Codes?
The UNII codes for the active ingredients in this product are:
- ROPINIROLE HYDROCHLORIDE (UNII: D7ZD41RZI9)
- ROPINIROLE (UNII: 030PYR8953) (Active Moiety)
Which are Ropinirole 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)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Ropinirole?
- RxCUI: 312845 - rOPINIRole HCl 0.25 MG Oral Tablet
- RxCUI: 312845 - ropinirole 0.25 MG Oral Tablet
- RxCUI: 312845 - ropinirole 0.25 MG (as ropinirole hydrochloride) Oral Tablet
- RxCUI: 312847 - rOPINIRole HCl 2 MG Oral Tablet
- RxCUI: 312847 - ropinirole 2 MG Oral Tablet
* 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".