NDC 36987-2350

Para Grass Pollen

Para Grass Pollen

Para Grass Pollen 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 Urochloa Mutica Pollen.

• Product ID: 36987-2350_5afe0fb9-ffff-4dc2-8f99-2654574c5d57
• NDC: 36987-2350
• Product Type: Human Prescription Drug
• Proprietary Name: Para Grass Pollen
• Generic Name: Para Grass Pollen
• 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: UROCHLOA MUTICA POLLEN
• Active Ingredient Strength: 20000 [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 36987-2350-1

5 mL in 1 VIAL, MULTI-DOSE (36987-2350-1)

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

NDC SPL Data Element Entries

NDC 36987-2350-4 [36987235004]

Para Grass Pollen 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 36987-2350-1 [36987235001]

Para Grass Pollen 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 36987-2350-2 [36987235002]

Para Grass Pollen 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 36987-2350-3 [36987235003]

Para Grass Pollen 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
UROCHLOA MUTICA POLLEN	20000 [PNU]/mL

OpenFDA Data

• SPL SET ID: 4a590321-5e7d-4af5-9a71-6741fe0e6e65
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 3ZO9YGZ8ZJ
• RxNorm Concept Unique ID - RxCUI:
  • 894794

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 "Para Grass Pollen" or generic name "Para Grass Pollen"

NDC	Brand Name	Generic Name
36987-2347	Para Grass Pollen	Para Grass Pollen
36987-2348	Para Grass Pollen	Para Grass Pollen
36987-2349	Para Grass Pollen	Para Grass Pollen
36987-2350	Para Grass Pollen	Para Grass Pollen
36987-2351	Para Grass Pollen	Para Grass Pollen
36987-2352	Para Grass Pollen	Para Grass Pollen
36987-2353	Para Grass Pollen	Para Grass Pollen
36987-2354	Para Grass Pollen	Para Grass Pollen