NDC 48951-2056

Berberis Urtica

Berberis Urtica

Berberis Urtica is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Berberis Vulgaris Root Bark; Urtica Urens.

• Product ID: 48951-2056_6a85ad01-813a-4d9c-e053-2991aa0a4f85
• NDC: 48951-2056
• Product Type: Human Otc Drug
• Proprietary Name: Berberis Urtica
• Generic Name: Berberis Urtica
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: BERBERIS VULGARIS ROOT BARK; URTICA URENS
• Active Ingredient Strength: 2 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-2056-1

10 AMPULE in 1 BOX (48951-2056-1) > 1 mL in 1 AMPULE

• Marketing Start Date: 2009-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-2056-1 [48951205601]

Berberis Urtica LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01

Drug Details

Active Ingredients

Ingredient	Strength
BERBERIS VULGARIS ROOT BARK	2 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 18114889-b21f-4ecf-9e40-6bc59e5570ad
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • IHN2NQ5OF9
  • 1TH8Q20J0U

NDC Crossover Matching brand name "Berberis Urtica" or generic name "Berberis Urtica"

NDC	Brand Name	Generic Name
48951-2056	Berberis Urtica	Berberis Urtica
48951-2057	Berberis Urtica	Berberis Urtica