NDC 70166-488 Atovaquone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70166-488?
What are the uses for Atovaquone?
Which are Atovaquone UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATOVAQUONE (UNII: Y883P1Z2LT)
- ATOVAQUONE (UNII: Y883P1Z2LT) (Active Moiety)
Which are Atovaquone 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- WATER (UNII: 059QF0KO0R)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Atovaquone?
- RxCUI: 308429 - atovaquone 750 MG in 5 mL Oral Suspension
- RxCUI: 308429 - atovaquone 150 MG/ML Oral Suspension
- RxCUI: 308429 - atovaquone 1500 MG per 10 ML Oral Suspension
- RxCUI: 308429 - atovaquone 750 MG per 5 ML Oral Suspension
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Patient Education
Atovaquone
Atovaquone is used to treat Pneumocystis jiroveci [Pneumocystis carinii] pneumonia (PCP; type of pneumonia most likely to affect people with human immunodeficiency virus [HIV]) in teenagers and adults. Atovaquone is also used to prevent PCP in teenagers and adults who cannot take another medication used for prevention. Atovaquone is in a class of medications called antiprotozoal agents. It works by stopping the growth of certain types of protozoa that can cause pneumonia.
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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".