NDC 63874-339 Naproxen Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63874 - Altura Pharmaceuticals, Inc.
- 63874-339 - Naproxen Sodium
Product Characteristics
BLUE (C48333)
OVAL (C48345)
CAPSULE (C48336)
14 MM
16 MM
19 MM
G;32;375
G;32;500
G;0;275
G;0
1
Product Packages
NDC Code 63874-339-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 63874-339-02
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 63874-339-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 63874-339-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 63874-339-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63874-339?
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 (UNII: 57Y76R9ATQ)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
- NAPROXEN SODIUM (UNII: 9TN87S3A3C)
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Naproxen Sodium?
- RxCUI: 198012 - naproxen 375 MG Oral Tablet
- RxCUI: 198013 - naproxen 250 MG Oral Tablet
- RxCUI: 198014 - naproxen 500 MG Oral Tablet
- RxCUI: 849398 - naproxen sodium 275 MG Oral Tablet
- RxCUI: 849398 - naproxen sodium 275 MG (as naproxen 250 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".