NDC 55648-154 Ropinirole Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-154 - Ropinirole Hydrochloride
Product Characteristics
Product Packages
NDC Code 55648-154-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-154-02
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-154-03
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-154-04
Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 55648-154?
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Ropinirole Hydrochloride?
- RxCUI: 283858 - rOPINIRole HCl 3 MG Oral Tablet
- RxCUI: 283858 - ropinirole 3 MG Oral Tablet
- RxCUI: 283858 - ropinirole 3 MG (as ropinirole hydrochloride) Oral Tablet
- RxCUI: 312845 - rOPINIRole HCl 0.25 MG Oral Tablet
- RxCUI: 312845 - ropinirole 0.25 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".