NDC 22840-5782

Brazil Nut

Bertholletia Excelsa

Brazil Nut is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Bertholletia Excelsa Whole.

• Product ID: 22840-5782_79ebe8af-3396-1b14-e053-2a91aa0a89ba
• NDC: 22840-5782
• Product Type: Non-standardized Allergenic
• Proprietary Name: Brazil Nut
• Generic Name: Bertholletia Excelsa
• Dosage Form: Solution
• Route of Administration: INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
• Marketing Start Date: 1981-09-15
• Marketing Category: BLA / BLA
• Application Number: BLA101833
• Labeler Name: Greer Laboratories, Inc.
• Substance Name: BERTHOLLETIA EXCELSA WHOLE
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 22840-5782-2

10 mL in 1 VIAL, MULTI-DOSE (22840-5782-2)

• Marketing Start Date: 1981-09-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 22840-5782-5 [22840578205]

Brazil Nut SOLUTION

• Marketing Category: BLA
• Application Number: BLA101833
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1981-09-15

NDC 22840-5782-2 [22840578202]

Brazil Nut SOLUTION

• Marketing Category: BLA
• Application Number: BLA101833
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1981-09-15

Drug Details

Active Ingredients

Ingredient	Strength
BERTHOLLETIA EXCELSA WHOLE	.05 g/mL

NDC Crossover Matching brand name "Brazil Nut" or generic name "Bertholletia Excelsa"

NDC	Brand Name	Generic Name
0268-6110	BRAZIL NUT	Brazil Nut
22840-5782	Brazil Nut	Bertholletia excelsa
36987-1530	Brazil Nut	Brazil Nut
36987-1531	Brazil Nut	Brazil Nut
36987-1532	Brazil Nut	Brazil Nut
36987-1533	Brazil Nut	Brazil Nut