NDC 63304-218 Oxymorphone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63304 - Ranbaxy Pharmaceuticals Inc.
- 63304-218 - Oxymorphone Hydrochloride
Product Characteristics
Product Packages
NDC Code 63304-218-05
Package Description: 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 63304-218-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 63304-218?
What are the uses for Oxymorphone Hydrochloride?
Which are Oxymorphone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYMORPHONE HYDROCHLORIDE (UNII: 5Y2EI94NBC)
- OXYMORPHONE (UNII: 9VXA968E0C) (Active Moiety)
Which are Oxymorphone Hydrochloride 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)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
What is the NDC to RxNorm Crosswalk for Oxymorphone Hydrochloride?
- RxCUI: 977874 - oxyMORphone HCl 10 MG 12HR Extended Release Oral Tablet
- RxCUI: 977874 - 12 HR oxymorphone hydrochloride 10 MG Extended Release Oral Tablet
- RxCUI: 977874 - oxymorphone hydrochloride 10 MG 12 HR Extended Release Oral Tablet
- RxCUI: 977894 - oxyMORphone HCl 15 MG 12HR Extended Release Oral Tablet
- RxCUI: 977894 - 12 HR oxymorphone hydrochloride 15 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".