NDC 67296-1237 Truvada
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67296 - Redpharm Drug, Inc.
- 67296-1237 - Truvada
Product Characteristics
Product Packages
NDC Code 67296-1237-3
Package Description: 3 TABLET, FILM COATED in 1 BOTTLE
NDC Code 67296-1237-4
Package Description: 4 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 67296-1237?
What are the uses for Truvada?
Which are Truvada UNII Codes?
The UNII codes for the active ingredients in this product are:
- EMTRICITABINE (UNII: G70B4ETF4S)
- EMTRICITABINE (UNII: G70B4ETF4S) (Active Moiety)
- TENOFOVIR DISOPROXIL FUMARATE (UNII: OTT9J7900I)
- TENOFOVIR ANHYDROUS (UNII: W4HFE001U5) (Active Moiety)
Which are Truvada 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:
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- WATER (UNII: 059QF0KO0R)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Truvada?
- RxCUI: 476556 - emtricitabine 200 MG / tenofovir disoproxil fumarate 300 MG Oral Tablet
- RxCUI: 476556 - emtricitabine 200 MG / tenofovir disoproxil fumarate 300 MG (tenofovir disoproxil 245 MG) 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".