NDC 71919-037

Ambra grisea

Ambergris

Ambra grisea is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Ambergris.

Product ID71919-037_7e3e06c4-b00f-5d77-e053-2991aa0a7cec
NDC71919-037
Product TypeHuman Otc Drug
Proprietary NameAmbra grisea
Generic NameAmbergris
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-04-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameAMBERGRIS
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-037-07

15 mL in 1 VIAL, GLASS (71919-037-07)
Marketing Start Date2010-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-037-08 [71919003708]

Ambra grisea LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-037-07 [71919003707]

Ambra grisea LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-037-10 [71919003710]

Ambra grisea LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

NDC 71919-037-09 [71919003709]

Ambra grisea LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-29

Drug Details

Active Ingredients

IngredientStrength
AMBERGRIS30 [hp_C]/mL

OpenFDA Data

SPL SET ID:835f3835-a9d9-4221-a829-cc276b06f57a
Manufacturer
UNII
UPC Code
  • 0740640214138
  • NDC Crossover Matching brand name "Ambra grisea" or generic name "Ambergris"

    NDCBrand NameGeneric Name
    0220-0221Ambra griseaAMBERGRIS
    15631-0023AMBRA GRISEAAMBRA GRISEA
    60512-7101AMBRA GRISEAAMBRA GRISEA
    68428-195Ambra griseaAMBERGRIS
    71919-037Ambra griseaAMBERGRIS
    64117-105Nervous CoughAMBERGRIS

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