NDC 63545-699

Erbium sulphuricum

Erbium Sulphuricum

Erbium sulphuricum is a Buccal; Oral; Sublingual Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Erbium Sulfate Octahydrate.

• Product ID: 63545-699_70bc64ea-6e27-77e7-e053-2991aa0a449d
• NDC: 63545-699
• Product Type: Human Otc Drug
• Proprietary Name: Erbium sulphuricum
• Generic Name: Erbium Sulphuricum
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2018-07-09
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: ERBIUM SULFATE OCTAHYDRATE
• Active Ingredient Strength: 1 [hp_M]/[hp_M]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 63545-699-01

730 [hp_M] in 1 VIAL, GLASS (63545-699-01)

• Marketing Start Date: 2018-07-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-699-01 [63545069901]

Erbium sulphuricum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-09
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ERBIUM SULFATE OCTAHYDRATE	1 [hp_M]/[hp_M]

OpenFDA Data

• SPL SET ID: 70bc64ea-6e26-77e7-e053-2991aa0a449d
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • 76R3969825