NDC 36987-1377

Tangerine

Tangerine

Tangerine 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 Tangerine.

• Product ID: 36987-1377_255e0c54-6613-460b-a91f-452fdfd0319d
• NDC: 36987-1377
• Product Type: Human Prescription Drug
• Proprietary Name: Tangerine
• Generic Name: Tangerine
• 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: TANGERINE
• 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],Fruit Proteins [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1377-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1377-2)

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

NDC SPL Data Element Entries

NDC 36987-1377-1 [36987137701]

Tangerine 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 36987-1377-3 [36987137703]

Tangerine 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 36987-1377-4 [36987137704]

Tangerine 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 36987-1377-2 [36987137702]

Tangerine 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
TANGERINE	.1 g/mL

OpenFDA Data

• SPL SET ID: 42a03973-e3db-49f2-9264-f76aa831c045
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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• RxNorm Concept Unique ID - RxCUI:
  • 892502
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  • 966633
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  • 901298
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  • 1012193
  • 904423
  • 1012166
  • 1011411
  • 1011417
  • 1010706
  • 1010708
  • 1010970
  • 1010976

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
36987-1374	Tangerine	Tangerine
36987-1375	Tangerine	Tangerine
36987-1376	Tangerine	Tangerine
36987-1377	Tangerine	Tangerine