NDC 16590-606 Kadian
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333 - VIOLET)
BLUE (C48333)
18 MM
KADIAN;30;MG
KADIAN;50;MG
Code Structure Chart
Product Details
What is NDC 16590-606?
What are the uses for Kadian?
Which are Kadian UNII Codes?
The UNII codes for the active ingredients in this product are:
- MORPHINE SULFATE (UNII: X3P646A2J0)
- MORPHINE (UNII: 76I7G6D29C) (Active Moiety)
Which are Kadian 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- DIETHYL PHTHALATE (UNII: UF064M00AF)
- TALC (UNII: 7SEV7J4R1U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
What is the NDC to RxNorm Crosswalk for Kadian?
- RxCUI: 892345 - morphine sulfate 30 MG Extended Release Oral Capsule
- RxCUI: 892345 - MS 30 MG Extended Release Oral Capsule
- RxCUI: 892352 - morphine sulfate 60 MG Extended Release Oral Capsule
- RxCUI: 892352 - morphine sulfate 60 MG 12-24 HR Extended Release Oral Capsule
- RxCUI: 892352 - MS 60 MG Extended Release Oral Capsule
* 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".