36987-2557 NDC - BOX ELDER ()

Drug Information

  • Product NDC: 36987-2557
  • Proprietary Name: Box Elder
  • 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
136987-2557-15 mL in 1 VIAL, MULTI-DOSE (36987-2557-1)
236987-2557-210 mL in 1 VIAL, MULTI-DOSE (36987-2557-2)
336987-2557-330 mL in 1 VIAL, MULTI-DOSE (36987-2557-3)
436987-2557-450 mL in 1 VIAL, MULTI-DOSE (36987-2557-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC36987-2557The translation of the dosage form Code submitted by the firm.
PROPRIETARY NAMEBox ElderThis is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE8/29/1972This 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.
MARKETING CATEGORY NAMEBLAName of Company corresponding to the labeler code segment of the Product NDC.
APPLICATION NUMBERBLA102192 
LABELER NAMENelco Laboratories, Inc. 

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

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