NDC 0360-0076

BRYONIA

Bryonia Alb.

BRYONIA is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Standard Homeopathic Company. The primary component is Bryonia Alba Root.

• Product ID: 0360-0076_7e04c62d-401d-6520-e053-2a91aa0afbfe
• NDC: 0360-0076
• Product Type: Human Otc Drug
• Proprietary Name: BRYONIA
• Generic Name: Bryonia Alb.
• Dosage Form: Tablet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1997-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: STANDARD HOMEOPATHIC COMPANY
• Substance Name: BRYONIA ALBA ROOT
• Active Ingredient Strength: 30 [hp_X]/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0360-0076-01

1 g in 1 BOTTLE, PLASTIC (0360-0076-01)

• Marketing Start Date: 1997-02-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0360-0076-01 [00360007601]

BRYONIA TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1997-02-17

Drug Details

Active Ingredients

Ingredient	Strength
BRYONIA ALBA ROOT	30 [hp_X]/g

OpenFDA Data

• SPL SET ID: 4b43a6d1-165a-6cc5-e054-00144ff88e88
• Manufacturer:
  • STANDARD HOMEOPATHIC COMPANY
• UNII:
  • T7J046YI2B
• UPC Code:
  • 0300360007610

NDC Crossover Matching brand name "BRYONIA" or generic name "Bryonia Alb."

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