NDC 59011-261 Ms Contin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59011 - Purdue Pharma Lp
- 59011-261 - Ms Contin
Product Characteristics
PURPLE (C48327 - LAVENDER)
PF;M30
Product Packages
NDC Code 59011-261-25
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Price per Unit: $6.71584 per EA
Product Details
What is NDC 59011-261?
What are the uses for Ms Contin?
Which are Ms Contin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MORPHINE SULFATE (UNII: X3P646A2J0)
- MORPHINE (UNII: 76I7G6D29C) (Active Moiety)
Which are Ms Contin 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) (UNII: 8136Y38GY5)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- LACTOSE (UNII: J2B2A4N98G)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Ms Contin?
- RxCUI: 891874 - morphine sulfate 100 MG Extended Release Oral Tablet
- RxCUI: 891874 - MS 100 MG Extended Release Oral Tablet
- RxCUI: 891881 - morphine sulfate 15 MG Extended Release Oral Tablet
- RxCUI: 891881 - MS 15 MG Extended Release Oral Tablet
- RxCUI: 891888 - morphine sulfate 30 MG Extended Release 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".