NDC 42494-407 Ec-naproxen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42494 - Cameron Pharmaceuticals, Llc
- 42494-407 - Ec-naproxen
Product Characteristics
PINK (C48328)
WHITE (C48325)
OVAL (C48345)
CAPSULE (C48336)
14 MM
16 MM
NPR;LE;375
NPR;LE;500
NPR;EC;375
1
Product Packages
NDC Code 42494-407-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 42494-407?
What are the uses for Ec-naproxen?
Which are Ec-naproxen UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN (UNII: 57Y76R9ATQ)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Ec-naproxen 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)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- TALC (UNII: 7SEV7J4R1U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ec-naproxen?
- RxCUI: 198012 - naproxen 375 MG Oral Tablet
- RxCUI: 198013 - naproxen 250 MG Oral Tablet
- RxCUI: 198014 - naproxen 500 MG Oral Tablet
- RxCUI: 311915 - naproxen 500 MG Delayed Release Oral Tablet
- RxCUI: 311915 - naproxen (as naproxen sodium) 500 MG Delayed Release 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".