NDC 36987-1489

Sweet Potato

Sweet Potato

Sweet Potato 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 Sweet Potato.

• Product ID: 36987-1489_255e0c54-6613-460b-a91f-452fdfd0319d
• NDC: 36987-1489
• Product Type: Human Prescription Drug
• Proprietary Name: Sweet Potato
• Generic Name: Sweet Potato
• 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: SWEET POTATO
• 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],Vegetable Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1489-4

50 mL in 1 VIAL, MULTI-DOSE (36987-1489-4)

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

NDC SPL Data Element Entries

NDC 36987-1489-1 [36987148901]

Sweet Potato 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 36987-1489-3 [36987148903]

Sweet Potato 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 36987-1489-2 [36987148902]

Sweet Potato 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 36987-1489-4 [36987148904]

Sweet Potato 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
SWEET POTATO	.1 g/mL

OpenFDA Data

• SPL SET ID: 42a03973-e3db-49f2-9264-f76aa831c045
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 892502
  • 904822
  • 1011032
  • 904628
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  • 891657
  • 899419
  • 1012120
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  • 1011075
  • 892371
  • 1011071
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  • 891663
  • 892677
  • 1011078
  • 966633
  • 904413
  • 904411
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  • 901385
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  • 1010848
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  • 891675
  • 1011065
  • 891779
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  • 902985
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  • 1010910
  • 1010914
  • 895579
  • 892520
  • 892529
  • 904438
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  • 1010702
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  • 892558
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  • 1011004
  • 904836
  • 901298
  • 895594
  • 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]
• Vegetable Proteins [CS]

NDC Crossover Matching brand name "Sweet Potato" or generic name "Sweet Potato"

NDC	Brand Name	Generic Name
0268-6205	SWEET POTATO	SWEET POTATO
22840-5743	Sweet Potato	Ipomoea batatas
36987-1486	Sweet Potato	Sweet Potato
36987-1487	Sweet Potato	Sweet Potato
36987-1488	Sweet Potato	Sweet Potato
36987-1489	Sweet Potato	Sweet Potato
49288-0388	Sweet Potato	Sweet Potato
54575-444	SWEET POTATO	sweet potato