NDC 70166-492 Oxycodone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70166 - Lohxa
- 70166-492 - Oxycodone Hydrochloride
Product Characteristics
Product Packages
NDC Code 70166-492-10
Package Description: 30 BAG in 1 CARTON / 1 SYRINGE in 1 BAG / .5 mL in 1 SYRINGE
NDC Code 70166-492-20
Package Description: 30 BAG in 1 CARTON / 1 SYRINGE in 1 BAG / 1 mL in 1 SYRINGE
Product Details
What is NDC 70166-492?
What are the uses for Oxycodone Hydrochloride?
Which are Oxycodone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYCODONE HYDROCHLORIDE (UNII: C1ENJ2TE6C)
- OXYCODONE (UNII: CD35PMG570) (Active Moiety)
Which are Oxycodone Hydrochloride 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)
- SORBITOL (UNII: 506T60A25R)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Oxycodone Hydrochloride?
- RxCUI: 1049615 - oxyCODONE HCl 20 MG in 1 mL Concentrate for Oral Solution
- RxCUI: 1049615 - oxycodone hydrochloride 20 MG/ML Oral Solution
- RxCUI: 1049615 - oxycodone hydrochloride 20 MG per 1 ML Concentrate for Oral Solution
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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".