NDC 49288-0476

Salmon

Salmon

Salmon 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 Atlantic Salmon.

• Product ID: 49288-0476_28463a0e-70af-4169-b592-df65f4f13a5f
• NDC: 49288-0476
• Product Type: Non-standardized Allergenic
• Proprietary Name: Salmon
• Generic Name: Salmon
• 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: ATLANTIC SALMON
• 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 49288-0476-5

50 mL in 1 VIAL, MULTI-DOSE (49288-0476-5)

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

NDC SPL Data Element Entries

NDC 49288-0476-4 [49288047604]

Salmon 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 49288-0476-1 [49288047601]

Salmon 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 49288-0476-5 [49288047605]

Salmon 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 49288-0476-2 [49288047602]

Salmon 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 49288-0476-3 [49288047603]

Salmon 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
ATLANTIC SALMON	.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 "Salmon" or generic name "Salmon"

NDC	Brand Name	Generic Name
0268-6212	SALMON	ATLANTIC SALMON
22840-5776	Salmon	Salmo salar
36987-1246	Salmon	Salmon
36987-1247	Salmon	Salmon
36987-1248	Salmon	Salmon
36987-1249	Salmon	Salmon
49288-0476	Salmon	Salmon