NDC 49288-0272

Jute

Jute

Jute 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 Corcorus Capsularis Fiber.

• Product ID: 49288-0272_3af4be6b-c022-4834-9006-f6cc8d8041da
• NDC: 49288-0272
• Product Type: Human Prescription Drug
• Proprietary Name: Jute
• Generic Name: Jute
• 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: CORCORUS CAPSULARIS FIBER
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Fiber Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Plant Proteins [CS],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0272-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0272-3)

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

NDC SPL Data Element Entries

NDC 49288-0272-3 [49288027203]

Jute 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 49288-0272-1 [49288027201]

Jute 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 49288-0272-4 [49288027204]

Jute 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 49288-0272-2 [49288027202]

Jute 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 49288-0272-5 [49288027205]

Jute 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
CORCORUS CAPSULARIS FIBER	.05 g/mL

OpenFDA Data

• SPL SET ID: d71013ab-718c-4cb0-ae1a-31fdd6db8851
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
  • 758Z9H9WV9
  • 70LDW53ROO
  • 6YR2608RSU
  • M30XO5X4XD
  • TVA75O7S63
• RxNorm Concept Unique ID - RxCUI:
  • 967973
  • 889598
  • 966928
  • 968497
  • 1098356
  • 904965
  • 852065
  • 1014199
  • 852547

Pharmacological Class

• Non-Standardized Plant Fiber Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Plant Proteins [CS]
• Allergens [CS]

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

NDC	Brand Name	Generic Name
36987-2246	Jute	Jute
36987-2247	Jute	Jute
36987-2248	Jute	Jute
36987-2249	Jute	Jute
36987-2250	Jute	Jute
36987-2251	Jute	Jute
36987-2252	Jute	Jute
36987-2253	Jute	Jute
49288-0272	Jute	Jute
49643-016	Jute	Jute