22840-1103 NDC - CATTLE EPITHELIA (BOS TAURUS)

Drug Information

Product NDC: 22840-1103
Proprietary Name: Cattle Epithelia
Non Proprietary Name: Bos taurus
Active Ingredient(s): .001 g/mL BOS TAURUS SKIN
Administration Route(s): INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): SOLUTION
Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Cells; Epidermal [EXT]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Animal Skin Allergenic Extract [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	Greer Laboratories, Inc.
Product Type:	NON-STANDARDIZED ALLERGENIC
FDA Application Number:	BLA101833
Marketing Category:	BLA
Start Marketing Date:	9/15/1981

Package Information

No.	Package Code	Package Description	Billing Unit
1	22840-1103-1	5 mL in 1 VIAL, MULTI-DOSE (22840-1103-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	22840-1103	The translation of the dosage form Code submitted by the firm.
PRODUCT TYPE NAME	NON-STANDARDIZED ALLERGENIC	This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAME	Cattle Epithelia	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Bos taurus	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.
DOSAGE FORM NAME	SOLUTION	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS	Name of Company corresponding to the labeler code segment of the Product NDC.
START MARKETING DATE	9/15/1981	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BLA	This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
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.
LABELER NAME	Greer Laboratories, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	BOS TAURUS SKIN	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.001
ACTIVE INGRED UNIT	g/mL
PHARM CLASSES	Allergens [CS], Cell-mediated Immunity [PE], Cells, Epidermal [EXT], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Animal Skin Allergenic Extract [EPC]

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This page was last updated on: 12/6/2025

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