NDC 54868-5413 Morphine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5413 - Morphine Sulfate
Product Packages
NDC Code 54868-5413-0
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 500 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 54868-5413?
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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Morphine Sulfate?
- RxCUI: 892589 - morphine sulfate 10 MG in 5 mL Oral Solution
- RxCUI: 892589 - morphine sulfate 2 MG/ML Oral Solution
- RxCUI: 892589 - morphine sulfate 10 MG per 5 ML Oral Solution
- RxCUI: 892589 - MS 2 MG/ML Oral Solution
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[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".