NDC 0121-2697 Naprosyn
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0121 - Pharmaceutical Associates, Inc.
- 0121-2697 - Naprosyn
Product Characteristics
Product Packages
NDC Code 0121-2697-22
Package Description: 10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 20 mL in 1 CUP, UNIT-DOSE (0121-2697-20)
Product Details
What is NDC 0121-2697?
What are the uses for Naprosyn?
Which are Naprosyn UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPROXEN (UNII: 57Y76R9ATQ)
- NAPROXEN (UNII: 57Y76R9ATQ) (Active Moiety)
Which are Naprosyn 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:
- SUCROSE (UNII: C151H8M554)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SORBITOL (UNII: 506T60A25R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- FUMARIC ACID (UNII: 88XHZ13131)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- PINEAPPLE (UNII: 2A88ZO081O)
- ORANGE (UNII: 5EVU04N5QU)
- WATER (UNII: 059QF0KO0R)
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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".