NDC 0268-6189

OYSTER

Eastern Oyster

OYSTER is a Percutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Eastern Oyster.

• Product ID: 0268-6189_1c2b4e7d-38fb-48f0-ad1a-1013ce4644ec
• NDC: 0268-6189
• Product Type: Non-standardized Allergenic
• Proprietary Name: OYSTER
• Generic Name: Eastern Oyster
• Dosage Form: Injection, Solution
• Route of Administration: PERCUTANEOUS
• Marketing Start Date: 1998-02-23
• Marketing Category: BLA / BLA
• Application Number: BLA103753
• Labeler Name: ALK-Abello, Inc.
• Substance Name: EASTERN OYSTER
• Active Ingredient Strength: 0 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0268-6189-10

10 mL in 1 VIAL (0268-6189-10)

• Marketing Start Date: 1998-02-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0268-6189-06 [00268618906]

OYSTER INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA103753
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1965-01-01

NDC 0268-6189-10 [00268618910]

OYSTER INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA103753
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1998-02-23

Drug Details

Active Ingredients

Ingredient	Strength
OYSTER, UNSPECIFIED	.1 g/mL

Pharmacological Class

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

NDC Crossover Matching brand name "OYSTER" or generic name "Eastern Oyster"

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