NDC 50192-113 Cambia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50192 - Nautilus Neurosciences, Inc.
- 50192-113 - Cambia
Product Characteristics
MINT (C73404)
Product Packages
NDC Code 50192-113-01
Package Description: 50 mg in 1 PACKET
NDC Code 50192-113-09
Package Description: 9 PACKET in 1 BOX / 50 mg in 1 PACKET
Price per Unit: $54.59753 per EA
Product Details
What is NDC 50192-113?
What are the uses for Cambia?
Which are Cambia UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC POTASSIUM (UNII: L4D5UA6CB4)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
Which are Cambia 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:
- ASPARTAME (UNII: Z0H242BBR1)
- GLYCERYL BEHENATE (UNII: R8WTH25YS2)
- MANNITOL (UNII: 3OWL53L36A)
- POTASSIUM BICARBONATE (UNII: HM5Z15LEBN)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Cambia?
- RxCUI: 859063 - diclofenac potassium 50 MG Powder for Oral Solution
- RxCUI: 859063 - Diclofenac K+ 50 MG Powder for Oral Solution
- RxCUI: 859063 - Diclofenac Pot 50 MG Powder for Oral Solution
- RxCUI: 859066 - CAMBIA 50 MG Powder for Oral Solution
- RxCUI: 859066 - diclofenac potassium 50 MG Powder for Oral Solution [Cambia]
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[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".