NDC 49288-0151

Currant

Currant

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

• Product ID: 49288-0151_80e3a713-b3c2-4981-9f01-d987196bc528
• NDC: 49288-0151
• Product Type: Human Prescription Drug
• Proprietary Name: Currant
• Generic Name: Currant
• 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: RED CURRANT
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Food Additives [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0151-5

50 mL in 1 VIAL, MULTI-DOSE (49288-0151-5)

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

NDC SPL Data Element Entries

NDC 49288-0151-4 [49288015104]

Currant INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0151-2 [49288015102]

Currant INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0151-1 [49288015101]

Currant INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0151-3 [49288015103]

Currant INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0151-5 [49288015105]

Currant INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
RED CURRANT	.05 g/mL

OpenFDA Data

• SPL SET ID: addbb916-198c-4992-98c3-a66b19a1e241
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
  • 81H2R5AOH3
  • Q5YG47WU3D
  • GH42T47V24
  • 5MG5Z946UO
• RxNorm Concept Unique ID - RxCUI:
  • 1014714
  • 1006343
  • 904501
  • 967981
  • 966699

Pharmacological Class

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