NDC 31722-338 Naproxen Delayed Release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 31722 - Camber Pharmaceuticals
- 31722-338 - Naproxen
Product Characteristics
Product Packages
NDC Code 31722-338-05
Package Description: 24 BOTTLE in 1 CASE / 100 TABLET in 1 BOTTLE (31722-338-01)
Product Details
What is NDC 31722-338?
What are the uses for Naproxen Delayed Release?
Which are Naproxen Delayed Release UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN (UNII: 57Y76R9ATQ)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Naproxen Delayed Release 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:
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Naproxen Delayed Release?
- RxCUI: 311915 - naproxen 500 MG Delayed Release Oral Tablet
- RxCUI: 311915 - naproxen (as naproxen sodium) 500 MG Delayed Release Oral Tablet
- RxCUI: 603103 - naproxen 375 MG Delayed Release Oral Tablet
- RxCUI: 603103 - naproxen 375 MG (as naproxen sodium 413 MG) Delayed Release 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".