NDC 16590-884 Ms Contin CR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-884 - Ms Contin
Product Characteristics
Product Packages
NDC Code 16590-884-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-884-56
Package Description: 56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-884-60
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-884-90
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 16590-884?
What are the uses for Ms Contin CR?
Which are Ms Contin CR 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 CR 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 CPS AT 5%) (UNII: 8136Y38GY5)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LACTOSE (UNII: J2B2A4N98G)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Ms Contin CR?
- RxCUI: 891893 - morphine sulfate 60 MG Extended Release Oral Tablet
- RxCUI: 891893 - MS 60 MG Extended Release Oral Tablet
- RxCUI: 894813 - MS Contin 60 MG Extended Release Oral Tablet
- RxCUI: 894813 - morphine sulfate 60 MG Extended Release Oral Tablet [MS Contin]
- RxCUI: 894813 - MS 60 MG Extended Release Oral Tablet [MS Contin]
* 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".