NDC 15631-0023

AMBRA GRISEA

Ambra Grisea

AMBRA GRISEA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Ambergris.

Product ID15631-0023_7b9f4414-7db8-4a59-89c4-4f805022b311
NDC15631-0023
Product TypeHuman Otc Drug
Proprietary NameAMBRA GRISEA
Generic NameAmbra Grisea
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAMBERGRIS
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0023-0

100 PELLET in 1 PACKAGE (15631-0023-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0023-3 [15631002303]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0023-0 [15631002300]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0023-1 [15631002301]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0023-4 [15631002304]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0023-5 [15631002305]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

NDC 15631-0023-2 [15631002302]

AMBRA GRISEA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-11

Drug Details

Active Ingredients

IngredientStrength
AMBERGRIS2 [hp_X]/1

OpenFDA Data

SPL SET ID:4bcd5010-0f8c-4a08-8f1d-6023810c45a7
Manufacturer
UNII

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

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

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