NDC 54458-865 Pioglitazone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54458 - International Laboratories, Llc
- 54458-865 - Pioglitazone
Product Characteristics
TEVA;7272
Product Packages
NDC Code 54458-865-10
Package Description: 30 TABLET in 1 BLISTER PACK
Price per Unit: $0.11701 per EA
Product Details
What is NDC 54458-865?
What are the uses for Pioglitazone?
Which are Pioglitazone UNII Codes?
The UNII codes for the active ingredients in this product are:
- PIOGLITAZONE HYDROCHLORIDE (UNII: JQT35NPK6C)
- PIOGLITAZONE (UNII: X4OV71U42S) (Active Moiety)
Which are Pioglitazone 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:
- CARBOXYMETHYLCELLULOSE CALCIUM (UNII: UTY7PDF93L)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
What is the NDC to RxNorm Crosswalk for Pioglitazone?
- RxCUI: 312440 - pioglitazone 30 MG Oral Tablet
- RxCUI: 312440 - pioglitazone (as pioglitazone hydrochloride) 30 MG Oral Tablet
- RxCUI: 312441 - pioglitazone 45 MG Oral Tablet
- RxCUI: 312441 - pioglitazone (as pioglitazone HCl) 45 MG Oral Tablet
- RxCUI: 317573 - pioglitazone 15 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".