NDC 69097-233 Nevirapine
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Product Details
What is NDC 69097-233?
What are the uses for Nevirapine?
Which are Nevirapine UNII Codes?
The UNII codes for the active ingredients in this product are:
- NEVIRAPINE HEMIHYDRATE (UNII: B7XF2TD73C)
- NEVIRAPINE (UNII: 99DK7FVK1H) (Active Moiety)
Which are Nevirapine 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Nevirapine?
- RxCUI: 311943 - nevirapine 50 MG in 5 mL Oral Suspension
- RxCUI: 311943 - nevirapine 10 MG/ML Oral Suspension
- RxCUI: 311943 - nevirapine (as nevirapine hemihydrate) 10 MG/ML Oral Suspension
- RxCUI: 311943 - nevirapine 50 MG per 5 ML Oral Suspension
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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".