NDC 21695-798 Ropinirole Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333)
8 MM
COR;207
Code Structure Chart
Product Details
What is NDC 21695-798?
What are the uses for Ropinirole Hydrochloride?
Which are Ropinirole Hydrochloride 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 Hydrochloride 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Ropinirole Hydrochloride?
- 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: 312849 - rOPINIRole HCl 5 MG Oral Tablet
- RxCUI: 312849 - ropinirole 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".