36987-2466 NDC - TAG ALDER ()

Drug Information

Product NDC: 36987-2466
Proprietary Name: Tag Alder
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

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

Package Information

No.	Package Code	Package Description	Billing Unit
1	36987-2466-1	5 mL in 1 VIAL, MULTI-DOSE (36987-2466-1)
2	36987-2466-2	10 mL in 1 VIAL, MULTI-DOSE (36987-2466-2)
3	36987-2466-3	30 mL in 1 VIAL, MULTI-DOSE (36987-2466-3)
4	36987-2466-4	50 mL in 1 VIAL, MULTI-DOSE (36987-2466-4)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	36987-2466	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	Tag Alder	Indicates 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.
START MARKETING DATE	8/29/1972	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAME	BLA	Product 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 NUMBER	BLA102192	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	Nelco Laboratories, Inc.	The translation of the route code submitted by the firm, indicating route of administration.

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This page was last updated on: 12/19/2025

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