NDC 49288-0570

Turkey

Turkey

Turkey 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 Turkey.

• Product ID: 49288-0570_ab729e90-03ec-4b3a-8c11-390b49ff5173
• NDC: 49288-0570
• Product Type: Human Prescription Drug
• Proprietary Name: Turkey
• Generic Name: Turkey
• 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: TURKEY
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Poultry Proteins [EXT],Non-Standardized Food Allergenic Extract [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0570-1

2 mL in 1 VIAL, MULTI-DOSE (49288-0570-1)

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

NDC SPL Data Element Entries

NDC 49288-0570-1 [49288057001]

Turkey 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 49288-0570-4 [49288057004]

Turkey 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 49288-0570-3 [49288057003]

Turkey 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 49288-0570-5 [49288057005]

Turkey 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 49288-0570-2 [49288057002]

Turkey 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
TURKEY	.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

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

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

NDC	Brand Name	Generic Name
0268-6229	TURKEY	TURKEY
36987-1166	Turkey	Turkey
36987-1167	Turkey	Turkey
36987-1168	Turkey	Turkey
36987-1169	Turkey	Turkey
49288-0570	Turkey	Turkey
54575-469	TURKEY FOOD	turkey