NDC 36987-1622

Watercress

Watercress

Watercress 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 Watercress.

• Product ID: 36987-1622_dec580ea-73db-4658-9de1-440c19bb42b7
• NDC: 36987-1622
• Product Type: Human Prescription Drug
• Proprietary Name: Watercress
• Generic Name: Watercress
• 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: WATERCRESS
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1622-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1622-3)

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

NDC SPL Data Element Entries

NDC 36987-1622-2 [36987162202]

Watercress 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 36987-1622-1 [36987162201]

Watercress 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 36987-1622-3 [36987162203]

Watercress 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 36987-1622-4 [36987162204]

Watercress 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
WATERCRESS	.05 g/mL

OpenFDA Data

• SPL SET ID: b65366b5-55ea-49dc-8011-8ef9af097291
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
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• RxNorm Concept Unique ID - RxCUI:
  • 891505
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  • 901294
  • 1010929
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  • 899381
  • 1011069
  • 904651
  • 899385
  • 899632
  • 1000013
  • 899737
  • 904487
  • 899733
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  • 1010918
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  • 904642
  • 891671
  • 899640
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  • 904533
  • 2103256
  • 891517
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  • 1006513
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  • 899417
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  • 899493
  • 899366
  • 892487
  • 899362
  • 1010700
  • 1011415
  • 899882
  • 1010974

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
36987-1622	Watercress	Watercress
36987-1623	Watercress	Watercress
36987-1624	Watercress	Watercress
36987-1625	Watercress	Watercress