NDC 49288-0189

Whole Egg

Whole Egg

Whole Egg 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 Egg.

• Product ID: 49288-0189_ab729e90-03ec-4b3a-8c11-390b49ff5173
• NDC: 49288-0189
• Product Type: Human Prescription Drug
• Proprietary Name: Whole Egg
• Generic Name: Whole Egg
• 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: EGG
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Egg Proteins, Dietary [CS],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0189-4

30 mL in 1 VIAL, MULTI-DOSE (49288-0189-4)

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

NDC SPL Data Element Entries

NDC 49288-0189-4 [49288018904]

Whole Egg 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 49288-0189-2 [49288018902]

Whole Egg 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 49288-0189-3 [49288018903]

Whole Egg 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 49288-0189-1 [49288018901]

Whole Egg 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 49288-0189-5 [49288018905]

Whole Egg 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
EGG	.05 g/mL

OpenFDA Data

• SPL SET ID: 422e7c71-ab7d-4064-97b9-a2d0527f18b0
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
  • O138UB266J
  • 4PIB2155QP
  • 28ON068RWM
  • XE5K5I4RP7
  • 85EA9K88OY
  • 3E0I92Z2GR
  • 291P45F896
  • 83DC4O5TD3
  • 0X8Q245Y7B
  • 8E9NT44R8I
  • FOF26T73HA
  • O5V0F26RUW
  • 917J3173FT
• RxNorm Concept Unique ID - RxCUI:
  • 892668
  • 905493
  • 966672
  • 904657
  • 966654
  • 899626
  • 967004
  • 966934
  • 892619
  • 1006349
  • 966942
  • 966649
  • 905333

Pharmacological Class

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

NDC Crossover Matching brand name "Whole Egg" or generic name "Whole Egg"

NDC	Brand Name	Generic Name
36987-1138	Whole Egg	Whole Egg
36987-1139	Whole Egg	Whole Egg
36987-1140	Whole Egg	Whole Egg
36987-1141	Whole Egg	Whole Egg
49288-0189	Whole Egg	Whole Egg
54575-390	WHOLE EGG	egg
0268-6135	EGG	Whole Egg