NDC 16590-942 Exalgo
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-942 - Exalgo
Product Characteristics
Product Packages
NDC Code 16590-942-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-942-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 16590-942-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 16590-942?
What are the uses for Exalgo?
Which are Exalgo UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROMORPHONE HYDROCHLORIDE (UNII: L960UP2KRW)
- HYDROMORPHONE (UNII: Q812464R06) (Active Moiety)
Which are Exalgo 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- LACTOSE, ANHYDROUS (UNII: 3SY5LH9PMK)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Exalgo?
- RxCUI: 902741 - HYDROmorphone HCl 8 MG 24HR Extended Release Oral Tablet
- RxCUI: 902741 - 24 HR hydromorphone hydrochloride 8 MG Extended Release Oral Tablet
- RxCUI: 902741 - hydromorphone hydrochloride 8 MG 24 HR Extended Release Oral Tablet
- RxCUI: 902743 - Exalgo 8 MG 24HR Extended Release Oral Tablet
- RxCUI: 902743 - 24 HR hydromorphone hydrochloride 8 MG Extended Release Oral Tablet [Exalgo]
* 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".