NDC 0220-0831

Berberis aquifolium

Berberis Aquifolium Root Bark

Berberis aquifolium is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Berberis Aquifolium Root Bark.

• Product ID: 0220-0831_6c422b8e-fa2a-a5b2-e053-2991aa0a27d8
• NDC: 0220-0831
• Product Type: Human Otc Drug
• Proprietary Name: Berberis aquifolium
• Generic Name: Berberis Aquifolium Root Bark
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: BERBERIS AQUIFOLIUM ROOT BARK
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-0831-41

30 [hp_C] in 1 TUBE (0220-0831-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-0831-41 [00220083141]

Berberis aquifolium PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
BERBERIS AQUIFOLIUM ROOT BARK	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 6c422b8e-fa29-a5b2-e053-2991aa0a27d8
• Manufacturer:
  • Boiron
• UNII:
  • VZJ9F3C3SB

NDC Crossover Matching brand name "Berberis aquifolium" or generic name "Berberis Aquifolium Root Bark"

NDC	Brand Name	Generic Name
0220-0831	Berberis aquifolium	BERBERIS AQUIFOLIUM ROOT BARK
15631-0079	BERBERIS AQUIFOLIUM	BERBERIS AQUIFOLIUM
15631-0538	BERBERIS AQUIFOLIUM	BERBERIS AQUIFOLIUM
68428-256	Berberis aquifolium	MAHONIA AQUIFOLIUM ROOT BARK
71919-119	Berberis aquifolium	BERBERIS AQUIFOLIUM ROOT BARK