NDC 0220-1601

Cuprum aceticum

Cupric Acetate

Cuprum aceticum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Cupric Acetate.

• Product ID: 0220-1601_7a2dfc0b-55da-5729-e053-2a91aa0abb3d
• NDC: 0220-1601
• Product Type: Human Otc Drug
• Proprietary Name: Cuprum aceticum
• Generic Name: Cupric Acetate
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: CUPRIC ACETATE
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-1601-41

30 [hp_C] in 1 TUBE (0220-1601-41)

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

NDC SPL Data Element Entries

NDC 0220-1601-41 [00220160141]

Cuprum aceticum PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
CUPRIC ACETATE	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 7a2dfc0b-55d9-5729-e053-2a91aa0abb3d
• Manufacturer:
  • Boiron
• UNII:
  • 39M11XPH03

NDC Crossover Matching brand name "Cuprum aceticum" or generic name "Cupric Acetate"

NDC	Brand Name	Generic Name
0220-1601	Cuprum aceticum	CUPRIC ACETATE
15631-0162	CUPRUM ACETICUM	CUPRUM ACETICUM
37662-0586	Cuprum Aceticum	Cuprum Aceticum
37662-0587	Cuprum Aceticum	Cuprum Aceticum
37662-0588	Cuprum Aceticum	Cuprum Aceticum
37662-0589	Cuprum Aceticum	Cuprum Aceticum
37662-0590	Cuprum Aceticum	Cuprum Aceticum
37662-0591	Cuprum Aceticum	Cuprum Aceticum
37662-0592	Cuprum Aceticum	Cuprum Aceticum
37662-0593	Cuprum Aceticum	Cuprum Aceticum
68428-928	Cuprum aceticum	CUPRIC ACETATE
71919-241	Cuprum aceticum	CUPRIC ACETATE