NDC 61480-124

Psorizide Ultra

Potassium Bromide, Nickel Sulfate, And Zinc Bromide

Psorizide Ultra is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Plymouth Healthcare Products Llc. The primary component is Potassium Bromide; Nickel Sulfate; Zinc Bromide.

• Product ID: 61480-124_3ed2138f-db38-4878-92b8-97b6d78f98e1
• NDC: 61480-124
• Product Type: Human Prescription Drug
• Proprietary Name: Psorizide Ultra
• Generic Name: Potassium Bromide, Nickel Sulfate, And Zinc Bromide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1997-10-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: PLYMOUTH HEALTHCARE PRODUCTS LLC
• Substance Name: POTASSIUM BROMIDE; NICKEL SULFATE; ZINC BROMIDE
• Active Ingredient Strength: 1 [hp_X]/1; [hp_X]/1; [hp_X]/1
• Pharm Classes: Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 61480-124-05

100 TABLET in 1 BOTTLE (61480-124-05)

• Marketing Start Date: 1997-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61480-124-05 [61480012405]

Psorizide Ultra TABLET

• Marketing Category: Unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1997-10-01

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM BROMIDE	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 78d05c25-6817-4763-b662-6dbb0625fa84
• Manufacturer:
  • PLYMOUTH HEALTHCARE PRODUCTS LLC
• UNII:
  • 4FLT4T3WUN
  • OSD78555ZM
  • OO7ZBU9703
• UPC Code:
  • 0361480124052

Pharmacological Class

• Copper Absorption Inhibitor [EPC]
• Decreased Copper Ion Absorption [PE]