NDC 16590-188 Piroxicam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-188 - Piroxicam
Product Characteristics
GREEN (C48329 - OLIVE)
93;757
Product Packages
NDC Code 16590-188-15
Package Description: 15 CAPSULE in 1 BOTTLE
NDC Code 16590-188-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 16590-188-60
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 16590-188-82
Package Description: 180 CAPSULE in 1 BOTTLE
NDC Code 16590-188-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 16590-188?
What are the uses for Piroxicam?
Which are Piroxicam UNII Codes?
The UNII codes for the active ingredients in this product are:
- PIROXICAM (UNII: 13T4O6VMAM)
- PIROXICAM (UNII: 13T4O6VMAM) (Active Moiety)
Which are Piroxicam 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Piroxicam?
- RxCUI: 198107 - piroxicam 10 MG Oral Capsule
- RxCUI: 198108 - piroxicam 20 MG Oral Capsule
* 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".