NDC 49288-0251

Halibut

Halibut

Halibut is a Intradermal; Subcutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Pacific Halibut.

• Product ID: 49288-0251_28463a0e-70af-4169-b592-df65f4f13a5f
• NDC: 49288-0251
• Product Type: Non-standardized Allergenic
• Proprietary Name: Halibut
• Generic Name: Halibut
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1974-03-23
• Marketing Category: BLA / BLA
• Application Number: BLA102223
• Labeler Name: Antigen Laboratories, Inc.
• Substance Name: PACIFIC HALIBUT
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fish Proteins, Dietary [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0251-2

5 mL in 1 VIAL, MULTI-DOSE (49288-0251-2)

• Marketing Start Date: 1974-03-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49288-0251-4 [49288025104]

Halibut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-29

NDC 49288-0251-1 [49288025101]

Halibut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-29

NDC 49288-0251-2 [49288025102]

Halibut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-29

NDC 49288-0251-5 [49288025105]

Halibut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-29

NDC 49288-0251-3 [49288025103]

Halibut INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
PACIFIC HALIBUT	.05 g/mL

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0268-6236	HALIBUT	ATLANTIC HALIBUT
0268-7130	HALIBUT	HIPPOGLOSSUS HIPPOGLOSSUS
36987-1218	Halibut	Halibut
36987-1219	Halibut	Halibut
36987-1220	Halibut	Halibut
36987-1221	Halibut	Halibut
49288-0251	Halibut	Halibut
49288-0252	Halibut	Halibut
54575-401	HALIBUT	pacific halibut