NDC 0220-0646

Aurum muriaticum natronum

Sodium Tetrachloroaurate

Aurum muriaticum natronum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Sodium Tetrachloroaurate.

• Product ID: 0220-0646_84f16e5d-25cd-371e-e053-2991aa0a50e1
• NDC: 0220-0646
• Product Type: Human Otc Drug
• Proprietary Name: Aurum muriaticum natronum
• Generic Name: Sodium Tetrachloroaurate
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: SODIUM TETRACHLOROAURATE
• Active Ingredient Strength: 200 [kp_C]/200[kp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-0646-41

200 [kp_C] in 1 TUBE (0220-0646-41)

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

NDC SPL Data Element Entries

NDC 0220-0646-41 [00220064641]

Aurum muriaticum natronum PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM TETRACHLOROAURATE	200 [kp_C]/200[kp_C]

OpenFDA Data

• SPL SET ID: 84f16e5d-25cc-371e-e053-2991aa0a50e1
• Manufacturer:
  • Boiron
• UNII:
  • 7FT6QUT299

NDC Crossover Matching brand name "Aurum muriaticum natronum" or generic name "Sodium Tetrachloroaurate"

NDC	Brand Name	Generic Name
0220-0646	Aurum muriaticum natronum	SODIUM TETRACHLOROAURATE
0220-0648	Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE
0220-0649	Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE
0220-0650	Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE
68428-242	Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE
71919-103	Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE