NDC 49288-0569

Tuna

Tuna

Tuna 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 Tuna.

• Product ID: 49288-0569_28463a0e-70af-4169-b592-df65f4f13a5f
• NDC: 49288-0569
• Product Type: Non-standardized Allergenic
• Proprietary Name: Tuna
• Generic Name: Tuna
• 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: TUNA
• 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 49288-0569-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0569-3)

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

NDC SPL Data Element Entries

NDC 49288-0569-3 [49288056903]

Tuna 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 49288-0569-1 [49288056901]

Tuna 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 49288-0569-4 [49288056904]

Tuna 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 49288-0569-2 [49288056902]

Tuna 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 49288-0569-5 [49288056905]

Tuna 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
TUNA	.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 "Tuna" or generic name "Tuna"

NDC	Brand Name	Generic Name
0268-6226	TUNA	NORTHERN BLUEFIN TUNA
22840-5780	Tuna	Thunnus albacares
49288-0569	Tuna	Tuna
54575-468	TUNA	tuna