NDC 36987-1102

Rabbit Epithelium

Rabbit Epithelium

Rabbit Epithelium 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 Oryctolagus Cuniculus Skin.

• Product ID: 36987-1102_d877e2c0-e17b-4d3e-ba6a-c2a3cd27e025
• NDC: 36987-1102
• Product Type: Human Prescription Drug
• Proprietary Name: Rabbit Epithelium
• Generic Name: Rabbit Epithelium
• 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: ORYCTOLAGUS CUNICULUS SKIN
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Animal Skin Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Cells, Epidermal [EXT],Allergens [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1102-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1102-3)

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

NDC SPL Data Element Entries

NDC 36987-1102-1 [36987110201]

Rabbit Epithelium 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 36987-1102-4 [36987110204]

Rabbit Epithelium 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 36987-1102-2 [36987110202]

Rabbit Epithelium 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 36987-1102-3 [36987110203]

Rabbit Epithelium 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
ORYCTOLAGUS CUNICULUS SKIN	.05 g/mL

OpenFDA Data

• SPL SET ID: 9f1e3612-f877-471c-88e0-41e41439ac15
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • X2W7CLE97T
  • 88VZV9HGT4
  • Z91WAU43WC
  • 83B65P4796
  • 9WN2H714TG
  • 390AN9GB09
  • 3K873H631W
  • 1FCM16V0FV
  • 7J12CD6O9L
  • 6LK42KUV6W
  • GM3H4U6QS8
  • 15XI414745
  • 3EM4VW6TQN
  • Y69HPD48AI
  • JLG9853E2P
• RxNorm Concept Unique ID - RxCUI:
  • 895459
  • 895187
  • 895073
  • 894940
  • 852842
  • 895282
  • 894786
  • 852666
  • 895198
  • 852255
  • 1006503
  • 852301
  • 895008
  • 895290
  • 892854

Pharmacological Class

• Non-Standardized Animal Skin Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Cells
• Epidermal [EXT]
• Allergens [CS]

NDC Crossover Matching brand name "Rabbit Epithelium" or generic name "Rabbit Epithelium"

NDC	Brand Name	Generic Name
36987-1097	Rabbit Epithelium	Rabbit Epithelium
36987-1098	Rabbit Epithelium	Rabbit Epithelium
36987-1099	Rabbit Epithelium	Rabbit Epithelium
36987-1100	Rabbit Epithelium	Rabbit Epithelium
36987-1101	Rabbit Epithelium	Rabbit Epithelium
36987-1102	Rabbit Epithelium	Rabbit Epithelium
36987-1103	Rabbit Epithelium	Rabbit Epithelium
36987-1104	Rabbit Epithelium	Rabbit Epithelium
0268-6319	RABBIT	Rabbit Epithelium
0268-6320	RABBIT	Rabbit Epithelium