NDC 36987-1193

Bluefish

Bluefish

Bluefish is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Bluefish.

• Product ID: 36987-1193_3483052b-e8ac-47fc-aa09-c1058d243ce2
• NDC: 36987-1193
• Product Type: Human Prescription Drug
• Proprietary Name: Bluefish
• Generic Name: Bluefish
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1972-08-29
• Marketing Category: BLA / BLA
• Application Number: BLA102192
• Labeler Name: Nelco Laboratories, Inc.
• Substance Name: BLUEFISH
• 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 36987-1193-4

50 mL in 1 VIAL, MULTI-DOSE (36987-1193-4)

• Marketing Start Date: 1972-08-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 36987-1193-3 [36987119303]

Bluefish INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1193-4 [36987119304]

Bluefish INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1193-2 [36987119302]

Bluefish INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1193-1 [36987119301]

Bluefish INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
BLUEFISH	.1 g/mL

OpenFDA Data

• SPL SET ID: 5cba32bc-49a0-4279-82c5-eb2a0f59c989
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 79U8P8X3Q5
• RxNorm Concept Unique ID - RxCUI:
  • 892283

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 "Bluefish" or generic name "Bluefish"

NDC	Brand Name	Generic Name
36987-1190	Bluefish	Bluefish
36987-1191	Bluefish	Bluefish
36987-1192	Bluefish	Bluefish
36987-1193	Bluefish	Bluefish