NDC 53808-0208 Atripla
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - Doh Central Pharmacy
- 53808-0208 - Atripla
Product Characteristics
Product Packages
NDC Code 53808-0208-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 53808-0208?
What are the uses for Atripla?
Which are Atripla UNII Codes?
The UNII codes for the active ingredients in this product are:
- EFAVIRENZ (UNII: JE6H2O27P8)
- EFAVIRENZ (UNII: JE6H2O27P8) (Active Moiety)
- EMTRICITABINE (UNII: G70B4ETF4S)
- EMTRICITABINE (UNII: G70B4ETF4S) (Active Moiety)
- TENOFOVIR DISOPROXIL FUMARATE (UNII: OTT9J7900I)
- TENOFOVIR ANHYDROUS (UNII: W4HFE001U5) (Active Moiety)
Which are Atripla 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Atripla?
- RxCUI: 643066 - efavirenz 600 MG / emtricitabine 200 MG / tenofovir disoproxil fumarate 300 MG Oral Tablet
- RxCUI: 643070 - ATRIPLA 600 MG / 200 MG / 300 MG Oral Tablet
- RxCUI: 643070 - efavirenz 600 MG / emtricitabine 200 MG / tenofovir disoproxil fumarate 300 MG Oral Tablet [Atripla]
- RxCUI: 643070 - Atripla 600/200/300 Oral Tablet
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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".