NDC 54868-4598 Hydromorphone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4598 - Hydromorphone Hydrochloride
Product Characteristics
WHITE (C48325 - OFF-WHITE)
ROUND (C48348)
TRIANGLE (C48353)
7 MM
8 MM
M;4
M;8
2
Product Packages
NDC Code 54868-4598-0
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-2
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-3
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-4
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-5
Package Description: 150 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-6
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4598-7
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-4598?
What are the uses for Hydromorphone Hydrochloride?
Which are Hydromorphone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROMORPHONE HYDROCHLORIDE (UNII: L960UP2KRW)
- HYDROMORPHONE (UNII: Q812464R06) (Active Moiety)
Which are Hydromorphone 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Hydromorphone Hydrochloride?
- RxCUI: 897696 - HYDROmorphone HCl 2 MG Oral Tablet
- RxCUI: 897696 - hydromorphone hydrochloride 2 MG Oral Tablet
- RxCUI: 897702 - HYDROmorphone HCl 4 MG Oral Tablet
- RxCUI: 897702 - hydromorphone hydrochloride 4 MG Oral Tablet
- RxCUI: 897710 - HYDROmorphone HCl 8 MG 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".