NDC 44911-0382

Bryonia

Bryonia (alba)

Bryonia is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Bryonia Alba Root.

• Product ID: 44911-0382_08abcc4a-4bb9-4e26-b53f-d6d766b73108
• NDC: 44911-0382
• Product Type: Human Otc Drug
• Proprietary Name: Bryonia
• Generic Name: Bryonia (alba)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-08-19
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: BRYONIA ALBA ROOT
• Active Ingredient Strength: 200 [hp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 44911-0382-1

30 mL in 1 BOTTLE, DROPPER (44911-0382-1)

• Marketing Start Date: 2016-08-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0382-1 [44911038201]

Bryonia LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-08-19

Drug Details

Active Ingredients

Ingredient	Strength
BRYONIA ALBA ROOT	200 [hp_C]/mL

OpenFDA Data

• SPL SET ID: f9a2b9f3-5e35-4c3a-a8ae-a7312118e4f0
• Manufacturer:
  • Energique, Inc.
• UNII:
  • T7J046YI2B

NDC Crossover Matching brand name "Bryonia" or generic name "Bryonia (alba)"

NDC	Brand Name	Generic Name
0220-0915	Bryonia	BRYONIA ALBA ROOT
0220-0939	Bryonia	BRYONIA ALBA ROOT
0220-0940	Bryonia	BRYONIA ALBA ROOT
0220-0941	Bryonia	BRYONIA ALBA ROOT
0220-0942	Bryonia	BRYONIA ALBA ROOT
0220-0943	Bryonia	BRYONIA ALBA ROOT
0220-0944	Bryonia	BRYONIA ALBA ROOT
0220-0945	Bryonia	BRYONIA ALBA ROOT
0220-0946	Bryonia	BRYONIA ALBA ROOT
0220-0947	Bryonia	BRYONIA ALBA ROOT
0220-0948	Bryonia	BRYONIA ALBA ROOT
0220-0949	Bryonia	BRYONIA ALBA ROOT
0360-0076	BRYONIA	BRYONIA ALB.
0360-0077	BRYONIA	BRYONIA ALB.
44911-0382	Bryonia	Bryonia (Alba)
55714-6107	Bryonia	Bryonia
55714-9019	Bryonia	Bryonia
63083-7108	Bryonia	Bryonia