NDC 69189-3624 Reyataz
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69189 - Avera Mckennan Hospital
- 69189-3624 - Reyataz
Product Characteristics
Product Packages
NDC Code 69189-3624-1
Package Description: 1 CAPSULE, GELATIN COATED in 1 DOSE PACK
Product Details
What is NDC 69189-3624?
What are the uses for Reyataz?
Which are Reyataz UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATAZANAVIR SULFATE (UNII: 4MT4VIE29P)
- ATAZANAVIR (UNII: QZU4H47A3S) (Active Moiety)
Which are Reyataz 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:
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN (UNII: 2G86QN327L)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- AMMONIA (UNII: 5138Q19F1X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- ALCOHOL (UNII: 3K9958V90M)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SHELLAC (UNII: 46N107B71O)
What is the NDC to RxNorm Crosswalk for Reyataz?
- RxCUI: 402094 - Reyataz 150 MG Oral Capsule
- RxCUI: 402094 - atazanavir 150 MG Oral Capsule [Reyataz]
- RxCUI: 402246 - atazanavir sulfate 150 MG Oral Capsule
- RxCUI: 402246 - atazanavir 150 MG Oral Capsule
- RxCUI: 402246 - atazanavir 150 MG (as atazanavir sulfate 170.8 MG) Oral Capsule
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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".