NDC 48951-2057

Berberis Urtica

Berberis Urtica

Berberis Urtica is a Oral Pellet 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: 48951-2057_6d8613e9-335a-13af-e053-2a91aa0ae1f3
• NDC: 48951-2057
• Product Type: Human Otc Drug
• Proprietary Name: Berberis Urtica
• Generic Name: Berberis Urtica
• Dosage Form: Pellet
• 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: 1 [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-2057-2

1350 PELLET in 1 BOTTLE, GLASS (48951-2057-2)

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

NDC SPL Data Element Entries

NDC 48951-2057-2 [48951205702]

Berberis Urtica PELLET

• 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	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: a063c6ea-020e-4059-9a6e-14428ce26b6f
• 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