NDC 36987-2359

Quack Grass

Quack Grass

Quack Grass is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Elymus Repens Pollen.

• Product ID: 36987-2359_46893e16-0a95-41cc-816f-c05a3a464967
• NDC: 36987-2359
• Product Type: Human Prescription Drug
• Proprietary Name: Quack Grass
• Generic Name: Quack Grass
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1972-08-29
• Marketing Category: BLA / BLA
• Application Number: BLA102192
• Labeler Name: Nelco Laboratories, Inc.
• Substance Name: ELYMUS REPENS POLLEN
• Active Ingredient Strength: 40000 [PNU]/mL
• Pharm Classes: Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-2359-2

10 mL in 1 VIAL, MULTI-DOSE (36987-2359-2)

• Marketing Start Date: 1972-08-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 36987-2359-2 [36987235902]

Quack Grass INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-2359-3 [36987235903]

Quack Grass INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-2359-4 [36987235904]

Quack Grass INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-2359-1 [36987235901]

Quack Grass INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ELYMUS REPENS POLLEN	40000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 97c8bed1-efbd-4af1-b242-85f80edeee5b
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 50HCQ1NYV5
  • 766QT72BK6
  • V003SHB7VK
  • GOA51670YV
  • 74PD8J616H
  • 577VA5B4HP
  • 2XO08315X1
  • FAY1Y90VJ9
  • 6AU0ZD8T1O
  • A7IKY24TR7
  • 7U437HHU5C
  • F1KAH8374D
  • 257GC6QO0Q
  • ON2T85TA2O
  • I6KAZ8AO1O
• RxNorm Concept Unique ID - RxCUI:
  • 889664
  • 1014697
  • 889563
  • 1044507
  • 1044244
  • 900014
  • 897353
  • 1044528
  • 899546
  • 992850
  • 900163
  • 1044614
  • 899978
  • 889527
  • 899592
  • 1044254

Pharmacological Class

• Non-Standardized Pollen Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Pollen [CS]
• Allergens [CS]

NDC Crossover Matching brand name "Quack Grass" or generic name "Quack Grass"

NDC	Brand Name	Generic Name
36987-2355	Quack Grass	Quack Grass
36987-2356	Quack Grass	Quack Grass
36987-2357	Quack Grass	Quack Grass
36987-2358	Quack Grass	Quack Grass
36987-2359	Quack Grass	Quack Grass
36987-2360	Quack Grass	Quack Grass
36987-2361	Quack Grass	Quack Grass
36987-2362	Quack Grass	Quack Grass
49288-0430	Quack Grass	Quack Grass
0268-1418	ELYMUS REPENS POLLEN	Quack Grass
0268-1419	ELYMUS REPENS POLLEN	Quack Grass
0268-1420	ELYMUS REPENS POLLEN	Quack Grass
0268-6657	ELYMUS REPENS POLLEN	Quack Grass