NDC 71205-397 Oseltamivir Phosphate
Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71205 - Proficient Rx Lp
- 71205-397 - Oseltamivir Phosphate
Product Characteristics
Product Packages
NDC Code 71205-397-10
Package Description: 10 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 71205-397?
What are the uses for Oseltamivir Phosphate?
What are Oseltamivir Phosphate Active Ingredients?
Which are Oseltamivir Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- OSELTAMIVIR PHOSPHATE (UNII: 4A3O49NGEZ)
- OSELTAMIVIR ACID (UNII: K6106LV5Q8) (Active Moiety)
Which are Oseltamivir Phosphate 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)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- POVIDONE K30 (UNII: U725QWY32X)
- SHELLAC (UNII: 46N107B71O)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Oseltamivir Phosphate?
- RxCUI: 312122 - oseltamivir phosphate 75 MG Oral Capsule
- RxCUI: 312122 - oseltamivir 75 MG Oral Capsule
- RxCUI: 312122 - oseltamivir (as oseltamivir phosphate) 75 MG Oral Capsule
Which are the Pharmacologic Classes for Oseltamivir Phosphate?
* Please review the disclaimer below.
Patient Education
Oseltamivir
Oseltamivir is used to treat some types of influenza infection ('flu') in adults, children, and infants (older than 2 weeks of age) who have had symptoms of the flu for no longer than 2 days. This medication is also used to prevent some types of flu in adults and children (older than 1 year of age) when they have spent time with someone who has the flu or when there is a flu outbreak. Oseltamivir is in a class of medications called neuraminidase inhibitors. It works by stopping the spread of the flu virus in the body. Oseltamivir helps shorten the time that flu symptoms such as a stuffy or runny nose, sore throat, cough, muscle or joint aches, tiredness, headache, fever, and chills last. Oseltamivir will not prevent bacterial infections, which may occur as a complication of the flu.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".