NDC 0220-1442

Cobaltum metallicum

Cobalt

Cobaltum metallicum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Cobalt.

• Product ID: 0220-1442_7a01df7a-284f-570c-e053-2991aa0a1320
• NDC: 0220-1442
• Product Type: Human Otc Drug
• Proprietary Name: Cobaltum metallicum
• Generic Name: Cobalt
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: COBALT
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-1442-41

30 [hp_C] in 1 TUBE (0220-1442-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-1442-41 [00220144241]

Cobaltum metallicum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
COBALT	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 7a01df7a-284e-570c-e053-2991aa0a1320
• Manufacturer:
  • Boiron
• UNII:
  • 3G0H8C9362

NDC Crossover Matching brand name "Cobaltum metallicum" or generic name "Cobalt"

NDC	Brand Name	Generic Name
0220-1442	Cobaltum metallicum	COBALT
15631-0144	COBALTUM METALLICUM	COBALTUM METALLICUM
37662-0441	Cobaltum Metallicum	Cobaltum Metallicum
37662-0442	Cobaltum Metallicum	Cobaltum Metallicum
37662-0443	Cobaltum Metallicum	Cobaltum Metallicum
37662-0444	Cobaltum Metallicum	Cobaltum Metallicum
37662-0445	Cobaltum Metallicum	Cobaltum Metallicum
37662-0446	Cobaltum Metallicum	Cobaltum Metallicum
37662-0447	Cobaltum Metallicum	Cobaltum Metallicum
37662-0448	Cobaltum Metallicum	Cobaltum Metallicum
68428-327	Cobaltum metallicum	COBALT
71919-209	Cobaltum metallicum	COBALT