NDC 15631-0058

ASAFOETIDA

Asafoetida

ASAFOETIDA 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 Asafetida.

Product ID15631-0058_972d651e-bd57-4674-bda7-6a3c7ec44769
NDC15631-0058
Product TypeHuman Otc Drug
Proprietary NameASAFOETIDA
Generic NameAsafoetida
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameASAFETIDA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0058-0

100 PELLET in 1 PACKAGE (15631-0058-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0058-4 [15631005804]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0058-3 [15631005803]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0058-1 [15631005801]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0058-5 [15631005805]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0058-0 [15631005800]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0058-2 [15631005802]

ASAFOETIDA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
ASAFETIDA1 [hp_X]/1

OpenFDA Data

SPL SET ID:fb7a7d07-16a4-47bd-9703-9135013d2d37
Manufacturer
UNII

NDC Crossover Matching brand name "ASAFOETIDA" or generic name "Asafoetida"

NDCBrand NameGeneric Name
0220-0572AsafoetidaFERULA ASSA-FOETIDA RESIN
0220-0573AsafoetidaFERULA ASSA-FOETIDA RESIN
0220-0574AsafoetidaFERULA ASSA-FOETIDA RESIN
15631-0058ASAFOETIDAASAFOETIDA
60512-6522ASAFOETIDAASAFOETIDA
68428-231AsafoetidaASAFETIDA
71919-091AsafoetidaFERULA ASSA-FOETIDA RESIN

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