NDC 36987-1221

Halibut

Halibut

Halibut 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 Pacific Halibut.

• Product ID: 36987-1221_398aea37-e253-4fd4-84ca-ca78367468b5
• NDC: 36987-1221
• Product Type: Human Prescription Drug
• Proprietary Name: Halibut
• Generic Name: Halibut
• 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: 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 36987-1221-4

50 mL in 1 VIAL, MULTI-DOSE (36987-1221-4)

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

NDC SPL Data Element Entries

NDC 36987-1221-3 [36987122103]

Halibut 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 36987-1221-1 [36987122101]

Halibut 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 36987-1221-2 [36987122102]

Halibut 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 36987-1221-4 [36987122104]

Halibut 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
PACIFIC HALIBUT	.1 g/mL

OpenFDA Data

• SPL SET ID: 026f2f1e-71cf-47ab-a24d-66663ff98429
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • BKZ683617P
  • 76780GX08D
  • 7062I37LB3
  • ZB2SV6JJY5
  • 0WLY635722
  • 01695YPV36
  • WF621S7K14
  • 5JKY494U4L
• RxNorm Concept Unique ID - RxCUI:
  • 905479
  • 892506
  • 905345
  • 892564
  • 904543
  • 901282
  • 892595
  • 892546
  • 966805
  • 899433
  • 966978
  • 901375
  • 904599
  • 901290
  • 899751
  • 899937
  • 905489
  • 901397
  • 905329
  • 892542
  • 905365
  • 892613

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