NDC 61715-060 Naproxen Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61715 - Kinray
- 61715-060 - Naproxen Sodium
Product Characteristics
Product Packages
NDC Code 61715-060-50
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 50 TABLET in 1 BOTTLE, PLASTIC
NDC Code 61715-060-51
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 100 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61715-060?
What are the uses for Naproxen Sodium?
Which are Naproxen Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN SODIUM (UNII: 9TN87S3A3C)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Naproxen Sodium 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Naproxen Sodium?
- RxCUI: 849574 - naproxen sodium 220 MG Oral Tablet
- RxCUI: 849574 - naproxen sodium 220 MG (as naproxen 200 MG) Oral Tablet
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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".