NDC 64725-0550 Invega
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0550 - Invega
Product Characteristics
Product Packages
NDC Code 64725-0550-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 64725-0550?
What are the uses for Invega?
Which are Invega UNII Codes?
The UNII codes for the active ingredients in this product are:
- PALIPERIDONE (UNII: 838F01T721)
- PALIPERIDONE (UNII: 838F01T721) (Active Moiety)
Which are Invega 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POVIDONES (UNII: FZ989GH94E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TRIACETIN (UNII: XHX3C3X673)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
What is the NDC to RxNorm Crosswalk for Invega?
- RxCUI: 672567 - paliperidone 3 MG 24HR Extended Release Oral Tablet
- RxCUI: 672567 - 24 HR paliperidone 3 MG Extended Release Oral Tablet
- RxCUI: 672567 - paliperidone 3 MG 24 HR Extended Release Oral Tablet
- RxCUI: 686441 - INVEGA 3 MG 24HR Extended Release Oral Tablet
- RxCUI: 686441 - 24 HR paliperidone 3 MG Extended Release Oral Tablet [Invega]
* 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".