NDC 49884-666 Morphine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325 - WHITE OPAQUE BODY)
BLUE (C48333 - BLUE VIOLET OPAQUE CAP)
16 MM
WATSON;3450;30;MG
Code Structure Chart
Product Details
What is NDC 49884-666?
What are the uses for Morphine Sulfate?
Which are Morphine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- MORPHINE SULFATE (UNII: X3P646A2J0)
- MORPHINE (UNII: 76I7G6D29C) (Active Moiety)
Which are Morphine Sulfate 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- DIETHYL PHTHALATE (UNII: UF064M00AF)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POVIDONE K30 (UNII: U725QWY32X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
What is the NDC to RxNorm Crosswalk for Morphine Sulfate?
- 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".