NDC 22840-5774

Oyster

Crassostrea Virginica

Oyster 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 Eastern Oyster.

• Product ID: 22840-5774_79ebe8af-3396-1b14-e053-2a91aa0a89ba
• NDC: 22840-5774
• Product Type: Non-standardized Allergenic
• Proprietary Name: Oyster
• Generic Name: Crassostrea Virginica
• 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: EASTERN OYSTER
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 22840-5774-2

10 mL in 1 VIAL, MULTI-DOSE (22840-5774-2)

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

NDC SPL Data Element Entries

NDC 22840-5774-5 [22840577405]

Oyster SOLUTION

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

NDC 22840-5774-2 [22840577402]

Oyster SOLUTION

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

Drug Details

Active Ingredients

Ingredient	Strength
EASTERN OYSTER	.05 g/mL

NDC Crossover Matching brand name "Oyster" or generic name "Crassostrea Virginica"

NDC	Brand Name	Generic Name
0268-6189	OYSTER	EASTERN OYSTER
22840-5774	Oyster	Crassostrea virginica
36987-1234	Oyster	Oyster
36987-1235	Oyster	Oyster
36987-1236	Oyster	Oyster
36987-1237	Oyster	Oyster
49288-0336	Oyster	Oyster