NDC 48951-9008

Thymus Mercurius

Thymus Mercurius

Thymus Mercurius is a Oral Liquid 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: 48951-9008_6ce59d2e-2a45-4951-e053-2a91aa0a25f7
• NDC: 48951-9008
• Product Type: Human Otc Drug
• Proprietary Name: Thymus Mercurius
• Generic Name: Thymus Mercurius
• 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: BOS TAURUS THYMUS; MERCURY
• Active Ingredient Strength: 8 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-9008-1

10 AMPULE in 1 BOX (48951-9008-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-9008-1 [48951900801]

Thymus Mercurius LIQUID

• 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]/mL

OpenFDA Data

• SPL SET ID: 28c34cbd-a0c2-4b6a-a923-acbfd75c840c
• 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