NDC 48951-9009

Thymus Mercurius

Thymus Mercurius

Thymus Mercurius is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Bos Taurus Thymus; Mercury.

• Product ID: 48951-9009_6e0e9ba8-2c25-0e2f-e053-2991aa0aa488
• NDC: 48951-9009
• Product Type: Human Otc Drug
• Proprietary Name: Thymus Mercurius
• Generic Name: Thymus Mercurius
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: BOS TAURUS THYMUS; MERCURY
• Active Ingredient Strength: 8 [hp_X]/1; [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-9009-2

1350 PELLET in 1 BOTTLE, GLASS (48951-9009-2)

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

NDC SPL Data Element Entries

NDC 48951-9009-2 [48951900902]

Thymus Mercurius PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
BOS TAURUS THYMUS	8 [hp_X]/1

OpenFDA Data

• SPL SET ID: e3abfd4c-a2c6-4154-9e8c-b8c59b87bc56
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • FXS1BY2PGL
  • 8XEJ88V2T8

NDC Crossover Matching brand name "Thymus Mercurius" or generic name "Thymus Mercurius"

NDC	Brand Name	Generic Name
48951-9008	Thymus Mercurius	Thymus Mercurius
48951-9009	Thymus Mercurius	Thymus Mercurius