36987-3211 NDC - GOLDENROD

Drug Information

Product NDC: 36987-3211

Proprietary Name: Goldenrod

Non Proprietary Name: Goldenrod

Active Ingredient(s):

Administration Route(s): INTRADERMAL; SUBCUTANEOUS


Pharmacy Class(es):
  • Non-Standardized Pollen Allergenic Extract [EPC];
  • Increased Histamine Release [PE];
  • Cell-mediated Immunity [PE];
  • Increased IgG Production [PE];
  • Pollen [CS];
  • Allergens [CS]

Labeler Information

Labeler Name: Nelco Laboratories, Inc.
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date:8/29/1972

Package Information

No. Package Code Package Description Billing Unit
136987-3211-15 mL in 1 VIAL, MULTI-DOSE (36987-3211-1)
236987-3211-210 mL in 1 VIAL, MULTI-DOSE (36987-3211-2)
336987-3211-330 mL in 1 VIAL, MULTI-DOSE (36987-3211-3)
436987-3211-450 mL in 1 VIAL, MULTI-DOSE (36987-3211-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC36987-3211The 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.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEGoldenrodThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGoldenrodThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTION, SOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRADERMAL; SUBCUTANEOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/29/1972This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEBLAProduct types are broken down into several potential Marketing Categories, such as NDA/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.
APPLICATION NUMBERBLA102192This 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 NAMENelco Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMESOLIDAGO CANADENSIS POLLENThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
PHARM CLASSESNon-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] 

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This page was last updated on: 9/13/2019