NDC 48951-2086

Bryonia Stannum

Bryonia Stannum

Bryonia Stannum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Bryonia Alba Root; Tin.

• Product ID: 48951-2086_6c7d9173-6897-3d99-e053-2a91aa0a9a3d
• NDC: 48951-2086
• Product Type: Human Otc Drug
• Proprietary Name: Bryonia Stannum
• Generic Name: Bryonia Stannum
• 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: BRYONIA ALBA ROOT; TIN
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-2086-1

10 AMPULE in 1 BOX (48951-2086-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-2086-1 [48951208601]

Bryonia Stannum LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
BRYONIA ALBA ROOT	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: e2a5de3e-526c-4a4b-9885-33c45d6f883a
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 387GMG9FH5
  • T7J046YI2B

NDC Crossover Matching brand name "Bryonia Stannum" or generic name "Bryonia Stannum"

NDC	Brand Name	Generic Name
48951-2086	Bryonia Stannum	Bryonia Stannum
48951-2087	Bryonia Stannum	Bryonia Stannum