NDC 78362-802 Viiva
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 78362-802?
What are the uses for Viiva?
Which are Viiva UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
Which are Viiva 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:
- WATER (UNII: 059QF0KO0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- ARGININE (UNII: 94ZLA3W45F)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- NIACINAMIDE (UNII: 25X51I8RD4)
- MELATONIN (UNII: JL5DK93RCL)
- LYSINE (UNII: K3Z4F929H6)
- ORNITHINE (UNII: E524N2IXA3)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
- PTEROCARPUS MARSUPIUM BARK (UNII: B6227M1TS0)
- MADECASSOSIDE (UNII: CQ2F5O6YIY)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
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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".