NDC 21695-905 Naprelan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 21695-905?
What are the uses for Naprelan?
Which are Naprelan UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN SODIUM (UNII: 9TN87S3A3C)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Naprelan 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Naprelan?
- RxCUI: 1116320 - naproxen sodium 375 MG 24HR Extended Release Oral Tablet
- RxCUI: 1116320 - 24 HR naproxen 375 MG Extended Release Oral Tablet
- RxCUI: 1116320 - naproxen 375 MG (naproxen sodium 413 MG) 24 HR Extended Release Oral Tablet
- RxCUI: 1116331 - NAPRELAN 375 MG 24HR Extended Release Oral Tablet
- RxCUI: 1116331 - 24 HR naproxen 375 MG Extended Release Oral Tablet [Naprelan]
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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".