Western Ragweed Mix

Ambrosia Acanthicarpa, Ambrosia Psilostachya

Greer Laboratories, Inc.
Non-standardized Allergenic
NDC 22840-9344

Western Ragweed Mix also known as Ambrosia Acanthicarpa, Ambrosia Psilostachya is a non standardized allergenic labeled by 'Greer Laboratories, Inc.'. National Drug Code (NDC) number for Western Ragweed Mix is 22840-9344. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Western Ragweed Mix drug includes Ambrosia Acanthicarpa Pollen - .0166666 g/mL Ambrosia Psilostachya Pollen - .0166666 g/mL . The currest status of Western Ragweed Mix drug is Active.

Drug Information:

Drug NDC:	22840-9344
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Western Ragweed Mix
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Non-standardized Allergenic
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Ambrosia Acanthicarpa, Ambrosia Psilostachya
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Greer Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	AMBROSIA ACANTHICARPA POLLEN - .0166666 g/mL AMBROSIA PSILOSTACHYA POLLEN - .0166666 g/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	INTRADERMAL PERCUTANEOUS SUBCUTANEOUS
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	BLA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date:	15 Sep, 1981
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	30 Dec, 2024
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number:	BLA101833
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
UNII:
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Non-Standardized Pollen Allergenic Extract [EPC] Pollen [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
22840-9344-2	10 mL in 1 VIAL, MULTI-DOSE (22840-9344-2)	15 Sep, 1981	N/A	No
22840-9344-4	50 mL in 1 VIAL, MULTI-DOSE (22840-9344-4)	15 Sep, 1981	N/A	No
22840-9344-5	5 mL in 1 BOTTLE, DROPPER (22840-9344-5)	15 Sep, 1981	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name
No other drugs with same generic name found.

Comments/ Reviews:

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