NDC 49288-0285

Kapok

Kapok

Kapok 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 Ceiba Pentandra Fiber.

• Product ID: 49288-0285_3af4be6b-c022-4834-9006-f6cc8d8041da
• NDC: 49288-0285
• Product Type: Human Prescription Drug
• Proprietary Name: Kapok
• Generic Name: Kapok
• 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: CEIBA PENTANDRA 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 49288-0285-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0285-3)

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

NDC SPL Data Element Entries

NDC 49288-0285-5 [49288028505]

Kapok 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 49288-0285-2 [49288028502]

Kapok 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 49288-0285-1 [49288028501]

Kapok 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 49288-0285-3 [49288028503]

Kapok 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 49288-0285-4 [49288028504]

Kapok 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
CEIBA PENTANDRA 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 "Kapok" or generic name "Kapok"

NDC	Brand Name	Generic Name
22840-1527	Kapok	Ceiba pentandra
22840-1529	Kapok	Ceiba pentandra
22840-1558	Kapok	Ceiba pentandra
22840-5514	Kapok	Ceiba pentandra
36987-2226	Kapok	Kapok
36987-2227	Kapok	Kapok
36987-2228	Kapok	Kapok
36987-2229	Kapok	Kapok
49288-0285	Kapok	Kapok
49643-017	Kapok	Kapok
54575-270	KAPOK	ceiba pentandra fiber
0268-0635	CEIBA PENTANDRA FIBER	KAPOK
0268-6312	CEIBA PENTANDRA FIBER	Kapok