NDC 54868-4476 Tamiflu
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4476 - Tamiflu
Product Characteristics
YELLOW (C48330 - LIGHT YELLOW)
18 MM
ROCHE;75;MG
Product Packages
NDC Code 54868-4476-0
Package Description: 1 BLISTER PACK in 1 CARTON / 10 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 54868-4476?
What are the uses for Tamiflu?
Which are Tamiflu UNII Codes?
The UNII codes for the active ingredients in this product are:
- OSELTAMIVIR PHOSPHATE (UNII: 4A3O49NGEZ)
- OSELTAMIVIR (UNII: 20O93L6F9H) (Active Moiety)
Which are Tamiflu 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:
- SORBITOL (UNII: 506T60A25R)
- MONOSODIUM CITRATE (UNII: 68538UP9SE)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- POVIDONE K30 (UNII: U725QWY32X)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- GELATIN (UNII: 2G86QN327L)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Tamiflu?
- RxCUI: 1115698 - oseltamivir phosphate 6 MG in 1 mL Oral Suspension
- RxCUI: 1115698 - oseltamivir 6 MG/ML Oral Suspension
- RxCUI: 1115698 - oseltamivir (as oseltamivir phosphate) 6 MG/ML Oral Suspension
- RxCUI: 1115698 - oseltamivir phosphate 6 MG per 1 ML Oral Suspension
- RxCUI: 1115700 - Tamiflu 6 MG in 1 mL Oral Suspension
* Please review the disclaimer below.
[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".