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  4. NDC Product Code: 44911-0551 Apizastat

NDC 44911-0551 Apizastat

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0551?
  4. Apizastat Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44911-0551
Proprietary Name:
Apizastat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
e9ecdbfd-45a1-4741-9a14-0f7011ac5905
Start Marketing Date: [9]
05-27-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 44911-0551?

The NDC code 44911-0551 is assigned by the FDA to the product Apizastat which is product labeled by Energique, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44911-0551-1 30 ml in 1 bottle, dropper . 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 Apizastat?

May temporarily relieve symptoms of fatigue, indigestion and abdominal pain with bloating.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms of fatigue, indigestion and abdominal pain with bloating.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Which are Apizastat 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)
  • BETA VULGARIS WHOLE (UNII: 4G174V5051)
  • BETA VULGARIS WHOLE (UNII: 4G174V5051) (Active Moiety)
  • MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
  • MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (Active Moiety)
  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (Active Moiety)
  • LARREA TRIDENTATA LEAF (UNII: PK0TXD049P)
  • LARREA TRIDENTATA LEAF (UNII: PK0TXD049P) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • URTICA DIOICA WHOLE (UNII: 710FLW4U46)
  • URTICA DIOICA WHOLE (UNII: 710FLW4U46) (Active Moiety)
  • VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172)
  • VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172) (Active Moiety)
  • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
  • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
  • OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0)
  • OXALIS ACETOSELLA LEAF (UNII: U1W3U02EW0) (Active Moiety)
  • SILVER (UNII: 3M4G523W1G)
  • SILVER (UNII: 3M4G523W1G) (Active Moiety)
  • CALCIUM FLUORIDE (UNII: O3B55K4YKI)
  • FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • THYMOL (UNII: 3J50XA376E)
  • THYMOL (UNII: 3J50XA376E) (Active Moiety)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • ALTERNANTHERA SESSILIS WHOLE (UNII: 5R502LRZ5J)
  • ALTERNANTHERA SESSILIS WHOLE (UNII: 5R502LRZ5J) (Active Moiety)
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P)
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (Active Moiety)

Which are Apizastat 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".