NDC 49288-0242 Mixture Of Standardized And Non-standardized Coastal Grasses

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:
49288-0242
Proprietary Name:
Mixture Of Standardized And Non-standardized Coastal Grasses
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Antigen Laboratories, Inc.
Labeler Code:
49288
Start Marketing Date: [9]
06-13-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49288-0242-3

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

NDC Code 49288-0242-4

Package Description: 30 mL in 1 VIAL, MULTI-DOSE

NDC Code 49288-0242-5

Package Description: 50 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 49288-0242?

The NDC code 49288-0242 is assigned by the FDA to the product Mixture Of Standardized And Non-standardized Coastal Grasses which is product labeled by Antigen Laboratories, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 49288-0242-3 10 ml in 1 vial, multi-dose , 49288-0242-4 30 ml in 1 vial, multi-dose , 49288-0242-5 50 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 Mixture Of Standardized And Non-standardized Coastal Grasses?

INDICATIONS AND USAGE     Allergenic extract is indicated for diagnostic testing and treatment (immunotherapy) of patients whose histories indicate allergic symptoms upon natural exposure to grass allergens. Confirmation is determined by skin testing. 10,000 BAU/ml extracts are intended for percutaneous testing. If negative, 100,000 BAU/ml products can be used for percutaneous test. Dilutions made from 10,000 BAU/ml products are indicated for immunotherapy of previously untreated patients. If 10,000 BAU/ml product is tolerated and symptoms persist, dilutions made from 100,000 BAU/ml can be administered. Standardized Grass Pollen extracts labeled in Bioequivalent Allergy Units (BAU/ml) are not interchangeable with grass pollen extracts labeled In Allergy Units (AU/ml) or with non-standardized grass pollen extracts.

Which are Mixture Of Standardized And Non-standardized Coastal Grasses UNII Codes?

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

  • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
  • FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
  • FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
  • DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P)
  • DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (Active Moiety)
  • AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA)
  • AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (Active Moiety)
  • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0)
  • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0) (Active Moiety)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
  • POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5)
  • POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5) (Active Moiety)
  • TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM)
  • TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM) (Active Moiety)
  • BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046)
  • BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (Active Moiety)
  • ZEA MAYS POLLEN (UNII: 74PD8J616H)
  • ZEA MAYS POLLEN (UNII: 74PD8J616H) (Active Moiety)
  • SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O)
  • SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O) (Active Moiety)
  • TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D)
  • TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (Active Moiety)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
  • ELYMUS REPENS POLLEN (UNII: ON2T85TA2O)
  • ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (Active Moiety)
  • PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9)
  • PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9) (Active Moiety)
  • BROMUS INERMIS POLLEN (UNII: 766QT72BK6)
  • BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (Active Moiety)
  • SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73)
  • SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73) (Active Moiety)
  • ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q)
  • ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q) (Active Moiety)
  • HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01)
  • HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (Active Moiety)
  • PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O)
  • PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (Active Moiety)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)

Which are Mixture Of Standardized And Non-standardized Coastal Grasses 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:

What is the NDC to RxNorm Crosswalk for Mixture Of Standardized And Non-standardized Coastal Grasses?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 851873 - redtop grass pollen extract 100000 BAU/ML Injectable Solution
  • RxCUI: 851873 - Agrostis gigantea pollen extract 100,000 BAU/ML Injectable Solution
  • RxCUI: 852157 - Timothy grass pollen extract 100000 BAU/mL Injectable Solution
  • RxCUI: 852157 - Timothy grass pollen extract 100000 BAU/ML Injectable Solution
  • RxCUI: 852157 - Phleum pratense grass pollen extract 100,000 BAU/ML Injectable Solution

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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".