NDC 63776-700 Growth Hormone

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63776-700
Proprietary Name:
Growth Hormone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Viatrexx Bio Incorporated
Labeler Code:
63776
Start Marketing Date: [9]
07-24-2012
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 63776-700-11

Package Description: 1 AMPULE in 1 BOX / .5 mL in 1 AMPULE

NDC Code 63776-700-14

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY

NDC Code 63776-700-15

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 50 mL in 1 BOTTLE, SPRAY

NDC Code 63776-700-16

Package Description: 1 BOTTLE in 1 BOX / 100 mL in 1 BOTTLE

NDC Code 63776-700-17

Package Description: 1 BOTTLE in 1 BOX / 250 mL in 1 BOTTLE

Product Details

What is NDC 63776-700?

The NDC code 63776-700 is assigned by the FDA to the product Growth Hormone which is product labeled by Viatrexx Bio Incorporated. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 63776-700-11 1 ampule in 1 box / .5 ml in 1 ampule, 63776-700-14 1 bottle, spray in 1 box / 30 ml in 1 bottle, spray, 63776-700-15 1 bottle, spray in 1 box / 50 ml in 1 bottle, spray, 63776-700-16 1 bottle in 1 box / 100 ml in 1 bottle, 63776-700-17 1 bottle in 1 box / 250 ml in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Growth Hormone?

This product is used as Growth HormoneHormonal support. To help with the support of health aging & vigor.

Which are Growth Hormone UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Growth Hormone 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:

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Product Footnotes

[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".