NDC 0220-0221

Ambra grisea

Ambergris

Ambra grisea is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Ambergris.

• Product ID: 0220-0221_687e64ac-7271-c2b2-e053-2a91aa0a1f4e
• NDC: 0220-0221
• Product Type: Human Otc Drug
• Proprietary Name: Ambra grisea
• Generic Name: Ambergris
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: AMBERGRIS
• Active Ingredient Strength: 6 [hp_C]/6[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-0221-41

6 [hp_C] in 1 TUBE (0220-0221-41)

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

NDC SPL Data Element Entries

NDC 0220-0221-41 [00220022141]

Ambra grisea PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
AMBERGRIS	6 [hp_C]/6[hp_C]

OpenFDA Data

• SPL SET ID: 687e64ac-7270-c2b2-e053-2a91aa0a1f4e
• Manufacturer:
  • Boiron
• UNII:
  • XTC0D02P6C

NDC Crossover Matching brand name "Ambra grisea" or generic name "Ambergris"

NDC	Brand Name	Generic Name
0220-0221	Ambra grisea	AMBERGRIS
15631-0023	AMBRA GRISEA	AMBRA GRISEA
60512-7101	AMBRA GRISEA	AMBRA GRISEA
68428-195	Ambra grisea	AMBERGRIS
71919-037	Ambra grisea	AMBERGRIS
64117-105	Nervous Cough	AMBERGRIS