NDC 49288-0808 Treatment Set Ts340153

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:
49288-0808
Proprietary Name:
Treatment Set Ts340153
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Antigen Laboratories, Inc.
Labeler Code:
49288
Start Marketing Date: [9]
10-31-1986
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49288-0808-3

Package Description: 10 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 49288-0808?

The NDC code 49288-0808 is assigned by the FDA to the product Treatment Set Ts340153 which is product labeled by Antigen Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49288-0808-3 10 ml in 1 vial, multi-dose . 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 Treatment Set Ts340153?

When the natural exposure to elevated aeroallergens produces symptoms as described under Clinical Pharmacology, specific diagnosis and therapeutic procedures are indicated. Clearly, important clues to the cause of a person's allergic condition can be gleaned from a thorough history and careful physical examination. Diagnostic tests - in vitro or in vivo - serve only to confirm the physician's suspicions or to improve investigative skills. Specific diagnosis is especially indicated when the patient's symptoms are not controlled by medication. When immunotherapy is contemplated demonstration of sensitivity to a specific allergenic extract is necessary. An orderly approach to the use of diagnostic tests usually begins with direct skin testing. 5,6,11THIS PRODUCT IS NOT INTENDED FOR TREATMENT OF PATIENTS WHO DO NOT MANIFEST IMMEDIATE HYPERSENSITIVITY REACTIONS TO THE ALLERGENIC EXTRACT FOLLOWING SKIN TESTING.

Which are Treatment Set Ts340153 UNII Codes?

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

  • FELIS CATUS HAIR (UNII: 1564HD0N96)
  • FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
  • CARYA ALBA POLLEN (UNII: G2A764T54B)
  • CARYA TOMENTOSA POLLEN (UNII: G2A764T54B) (Active Moiety)
  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)
  • DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K)
  • DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K) (Active Moiety)
  • CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
  • CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
  • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
  • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
  • ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
  • ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22) (Active Moiety)
  • CARYA TOMENTOSA POLLEN (UNII: G2A764T54B)
  • CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y)
  • CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (Active Moiety)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (Active Moiety)
  • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK)
  • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (Active Moiety)

Which are Treatment Set Ts340153 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:

* Please review the disclaimer below.

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".