NDC 48951-5068

Ignatia Bryophyllum

Ignatia Bryophyllum

Ignatia Bryophyllum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Kalanchoe Daigremontiana Leaf; Strychnos Ignatii Seed; Silver; Lachesis Muta Venom.

• Product ID: 48951-5068_55c75bfa-3564-293c-e054-00144ff88e88
• NDC: 48951-5068
• Product Type: Human Otc Drug
• Proprietary Name: Ignatia Bryophyllum
• Generic Name: Ignatia Bryophyllum
• 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: KALANCHOE DAIGREMONTIANA LEAF; STRYCHNOS IGNATII SEED; SILVER; LACHESIS MUTA VENOM
• Active Ingredient Strength: 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-5068-1

10 AMPULE in 1 BOX (48951-5068-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-5068-1 [48951506801]

Ignatia Bryophyllum LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
KALANCHOE DAIGREMONTIANA LEAF	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 4e8711b9-5623-43aa-ad8e-1d6893c09999
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 1NM3M2487K
  • VSW71SS07I
  • L6X13JKL8O
  • 3M4G523W1G

NDC Crossover Matching brand name "Ignatia Bryophyllum" or generic name "Ignatia Bryophyllum"

NDC	Brand Name	Generic Name
48951-5068	Ignatia Bryophyllum	Ignatia Bryophyllum
48951-5069	Ignatia Bryophyllum	Ignatia Bryophyllum
48951-8306	Ignatia Bryophyllum	Ignatia Bryophyllum