NDC 63545-659

Ferrum Bromatum

Ferrum Bromatum

Ferrum Bromatum 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 Ferrous Bromide.

• Product ID: 63545-659_44bb6a20-2151-417e-e054-00144ff8d46c
• NDC: 63545-659
• Product Type: Human Otc Drug
• Proprietary Name: Ferrum Bromatum
• Generic Name: Ferrum Bromatum
• Dosage Form: Pellet
• Route of Administration: BUCCAL; ORAL; SUBLINGUAL
• Marketing Start Date: 2016-12-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Hahnemann Laboratories, Inc.
• Substance Name: FERROUS BROMIDE
• Active Ingredient Strength: 30 [hp_C]/[hp_C]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 63545-659-01

240 [hp_C] in 1 VIAL, GLASS (63545-659-01)

• Marketing Start Date: 2016-12-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63545-659-01 [63545065901]

Ferrum Bromatum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-12-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
FERROUS BROMIDE	30 [hp_C]/[hp_C]

OpenFDA Data

• SPL SET ID: 44bb6a20-2150-417e-e054-00144ff8d46c
• Manufacturer:
  • Hahnemann Laboratories, Inc.
• UNII:
  • EA3X054RBZ

NDC Crossover Matching brand name "Ferrum Bromatum" or generic name "Ferrum Bromatum"

NDC	Brand Name	Generic Name
15631-0189	FERRUM BROMATUM	FERRUM BROMATUM
37662-0650	Ferrum Bromatum	Ferrum Bromatum
37662-0651	Ferrum Bromatum	Ferrum Bromatum
37662-0652	Ferrum Bromatum	Ferrum Bromatum
37662-0653	Ferrum Bromatum	Ferrum Bromatum
37662-0654	Ferrum Bromatum	Ferrum Bromatum
37662-0655	Ferrum Bromatum	Ferrum Bromatum
37662-0656	Ferrum Bromatum	Ferrum Bromatum
63545-659	Ferrum Bromatum	Ferrum Bromatum