NDC 36987-2226

Kapok

Kapok

Kapok 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 Ceiba Pentandra Fiber.

• Product ID: 36987-2226_ec73bb3c-d08d-4a3b-92a9-d2bfd09da169
• NDC: 36987-2226
• Product Type: Human Prescription Drug
• Proprietary Name: Kapok
• Generic Name: Kapok
• 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: 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 36987-2226-3

30 mL in 1 VIAL, MULTI-DOSE (36987-2226-3)

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

NDC SPL Data Element Entries

NDC 36987-2226-3 [36987222603]

Kapok 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 36987-2226-4 [36987222604]

Kapok 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 36987-2226-2 [36987222602]

Kapok 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 36987-2226-1 [36987222601]

Kapok 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
CEIBA PENTANDRA FIBER	.05 g/mL

OpenFDA Data

• SPL SET ID: 0fb71326-54c9-4139-befe-06ca832d02c8
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • 70LDW53ROO
  • 4110YT348C
  • M30XO5X4XD
  • MRJ91HVV4H
  • DI0ZRJ0MXN
  • TVA75O7S63
  • 758Z9H9WV9
  • 6YR2608RSU
• RxNorm Concept Unique ID - RxCUI:
  • 904846
  • 889598
  • 966928
  • 1098356
  • 904681
  • 966958
  • 978958
  • 904965
  • 1014199

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