NDC 36987-1770

Chestnut

Chestnut

Chestnut 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 American Chestnut.

• Product ID: 36987-1770_a0de52d8-af70-4f43-8468-3b7a42072d2f
• NDC: 36987-1770
• Product Type: Human Prescription Drug
• Proprietary Name: Chestnut
• Generic Name: Chestnut
• 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: AMERICAN CHESTNUT
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Nut Proteins [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1770-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1770-1)

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

NDC SPL Data Element Entries

NDC 36987-1770-1 [36987177001]

Chestnut 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 36987-1770-4 [36987177004]

Chestnut 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 36987-1770-3 [36987177003]

Chestnut 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 36987-1770-2 [36987177002]

Chestnut 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
AMERICAN CHESTNUT	.05 g/mL

OpenFDA Data

• SPL SET ID: 3712e1ea-6aaa-4ea5-b350-bdccfd30dde9
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 0XH1TH76XZ
• RxNorm Concept Unique ID - RxCUI:
  • 891755

Pharmacological Class

• Non-Standardized Plant Allergenic Extract [EPC]
• Non-Standardized Food Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Allergens [CS]
• Dietary Proteins [CS]
• Plant Proteins [CS]
• Nut Proteins [EXT]

NDC Crossover Matching brand name "Chestnut" or generic name "Chestnut"

NDC	Brand Name	Generic Name
36987-1770	Chestnut	Chestnut
36987-1771	Chestnut	Chestnut
36987-1772	Chestnut	Chestnut
36987-1773	Chestnut	Chestnut