NDC 44911-0097

Psorinum

Psorinum

Psorinum is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Scabies Lesion Lysate (human).

• Product ID: 44911-0097_0e27dae5-db51-4f1a-b12c-c3d8b3576a11
• NDC: 44911-0097
• Product Type: Human Prescription Drug
• Proprietary Name: Psorinum
• Generic Name: Psorinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-12-09
• Marketing End Date: 2025-09-22
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: SCABIES LESION LYSATE (HUMAN)
• Active Ingredient Strength: 7 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 44911-0097-1

30 mL in 1 PACKAGE (44911-0097-1)

• Marketing Start Date: 2014-12-09
• Marketing End Date: 2025-09-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0097-1 [44911009701]

Psorinum LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-12-09
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SCABIES LESION LYSATE (HUMAN)	7 [hp_X]/mL

OpenFDA Data

• SPL SET ID: fe712217-e56d-49f7-a791-0351f5e61896
• Manufacturer:
  • Energique, Inc.
• UNII:
  • 5UAU16Z1U4

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

NDC	Brand Name	Generic Name
0220-7604	Psorinum	SCABIES LESION LYSATE (HUMAN)
0220-7622	Psorinum	SCABIES LESION LYSATE (HUMAN)
0220-7623	Psorinum	SCABIES LESION LYSATE (HUMAN)
0220-7624	Psorinum	SCABIES LESION LYSATE (HUMAN)
0220-7625	Psorinum	SCABIES LESION LYSATE (HUMAN)
0220-7626	Psorinum	SCABIES LESION LYSATE (HUMAN)
44911-0097	Psorinum	Psorinum
62106-6903	PSORINUM	Psorinum
64117-407	PSORINUM	SCABIES LESION LYSATE (HUMAN)
69152-1204	Psorinum 1M	Psorinum
69152-1006	Psorinum 200C	Psorinum