NDC 63776-189 Viatrexx-gi
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 63776-189 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 63776-189?
What are the uses for Viatrexx-gi?
Which are Viatrexx-gi UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
- SUS SCROFA COLON (UNII: 94J255A0UC)
- SUS SCROFA COLON (UNII: 94J255A0UC) (Active Moiety)
- BOS TAURUS COLON (UNII: 8PD5L21RYS)
- BOS TAURUS COLON (UNII: 8PD5L21RYS) (Active Moiety)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R)
- FRANGULA ALNUS BARK (UNII: S2D77IH61R) (Active Moiety)
- INTERLEUKIN-12 HUMAN (UNII: 7B590791ER)
- INTERLEUKIN-12 HUMAN (UNII: 7B590791ER) (Active Moiety)
- INTERFERON GAMMA-1A (UNII: VC9M78242P)
- INTERFERON GAMMA-1A (UNII: VC9M78242P) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- BOS TAURUS PEYER'S PATCH (UNII: XB9AHC8DW1)
- BOS TAURUS PEYER'S PATCH (UNII: XB9AHC8DW1) (Active Moiety)
- SUS SCROFA PEYER'S PATCH (UNII: 308LM01C72)
- SUS SCROFA PEYER'S PATCH (UNII: 308LM01C72) (Active Moiety)
- SUS SCROFA RECTUM (UNII: QV1358E70N)
- SUS SCROFA RECTUM (UNII: QV1358E70N) (Active Moiety)
- SEROTONIN (UNII: 333DO1RDJY)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- VITAMIN D (UNII: 9VU1KI44GP) (Active Moiety)
Which are Viatrexx-gi 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".