NDC 50845-0113 Testosterone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50845 - Liddell Laboratories, Inc.
- 50845-0113 - Testosterone
Product Packages
NDC Code 50845-0113-3
Package Description: 1 CARTON in 1 CARTON / 1 BOTTLE, SPRAY in 1 CARTON (50845-0113-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0113-1)
Product Details
What is NDC 50845-0113?
What are the uses for Testosterone?
Which are Testosterone UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE) (Active Moiety)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) (Active Moiety)
- TESTOSTERONE (UNII: 3XMK78S47O)
- TESTOSTERONE (UNII: 3XMK78S47O) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- NUPHAR LUTEUM ROOT (UNII: 714LIU3V6D)
- NUPHAR LUTEUM ROOT (UNII: 714LIU3V6D) (Active Moiety)
- BOS TAURUS TESTICLE (UNII: PR4RXL6G2H)
- BOS TAURUS TESTICLE (UNII: PR4RXL6G2H) (Active Moiety)
Which are Testosterone 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".