NDC 36987-1651

Malt

Malt

Malt 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 Malt Extract, Barley.

• Product ID: 36987-1651_c9d2ad91-0541-4504-a528-c0cc93a99e4e
• NDC: 36987-1651
• Product Type: Human Prescription Drug
• Proprietary Name: Malt
• Generic Name: Malt
• 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: MALT EXTRACT, BARLEY
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Grain Proteins [EXT]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1651-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1651-3)

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

NDC SPL Data Element Entries

NDC 36987-1651-4 [36987165104]

Malt 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 36987-1651-2 [36987165102]

Malt 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 36987-1651-3 [36987165103]

Malt 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 36987-1651-1 [36987165101]

Malt 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
MALT EXTRACT, BARLEY	.05 g/mL

OpenFDA Data

• SPL SET ID: 9cf0d617-467d-461f-b6d3-d2d926982bb7
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 891505
  • 895581
  • 901340
  • 900050
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  • 891636
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  • 904479
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  • 899741
  • 966639
  • 899745
  • 904868
  • 899909
  • 1011046
  • 901294
  • 1010929
  • 1011063
  • 899389
  • 899381
  • 1011069
  • 904651
  • 899385
  • 899632
  • 1000013
  • 899737
  • 904487
  • 899733
  • 1010858
  • 895573
  • 895577
  • 1010850
  • 1010918
  • 1010854
  • 1010856
  • 904649
  • 904642
  • 891671
  • 899640
  • 901320
  • 1011020
  • 899401
  • 901202
  • 899483
  • 899880
  • 899727
  • 966699
  • 899886
  • 891679
  • 904533
  • 2103256
  • 891517
  • 891690
  • 1006513
  • 895591
  • 899655
  • 1011002
  • 899417
  • 899898
  • 899493
  • 899366
  • 892487
  • 899362
  • 1010700
  • 1011415
  • 899882
  • 1010974

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
22840-5729	Malt	Hordeum vulgare
36987-1650	Malt	Malt
36987-1651	Malt	Malt
36987-1652	Malt	Malt
36987-1653	Malt	Malt
49288-0292	Malt	Malt