NDC 60512-7101

AMBRA GRISEA

Ambra Grisea

AMBRA GRISEA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Ambergris.

• Product ID: 60512-7101_cafb8adf-a8f6-46f1-8183-552091dffe21
• NDC: 60512-7101
• Product Type: Human Otc Drug
• Proprietary Name: AMBRA GRISEA
• Generic Name: Ambra Grisea
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: AMBERGRIS
• Active Ingredient Strength: 2 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-7101-1

80 PELLET in 1 TUBE (60512-7101-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-7101-1 [60512710101]

AMBRA GRISEA PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
AMBERGRIS	2 [hp_X]/1

OpenFDA Data

• SPL SET ID: 74c58419-30be-4d7d-993c-bd06e2de3578
• Manufacturer:
  • HOMEOLAB USA INC.
• UNII:
  • XTC0D02P6C

NDC Crossover Matching brand name "AMBRA GRISEA" or generic name "Ambra Grisea"

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