NDC 15631-0059

ASARUM EUROPAEUM

Asarum Europaeum

ASARUM EUROPAEUM 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 Asarum Europaeum.

Product ID15631-0059_9ec84841-511c-66d8-e053-2995a90a3680
NDC15631-0059
Product TypeHuman Otc Drug
Proprietary NameASARUM EUROPAEUM
Generic NameAsarum Europaeum
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 NameASARUM EUROPAEUM
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0059-0

100 PELLET in 1 PACKAGE (15631-0059-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0059-2 [15631005902]

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

NDC 15631-0059-4 [15631005904]

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

NDC 15631-0059-1 [15631005901]

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

NDC 15631-0059-3 [15631005903]

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

NDC 15631-0059-5 [15631005905]

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

NDC 15631-0059-0 [15631005900]

ASARUM EUROPAEUM 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
ASARUM EUROPAEUM1 [hp_X]/1

OpenFDA Data

SPL SET ID:ab5905da-831d-4a78-b914-04086b5449ea
Manufacturer
UNII

NDC Crossover Matching brand name "ASARUM EUROPAEUM" or generic name "Asarum Europaeum"

NDCBrand NameGeneric Name
0220-0577Asarum europaeumASARUM EUROPAEUM
0220-0580Asarum europaeumASARUM EUROPAEUM
15631-0059ASARUM EUROPAEUMASARUM EUROPAEUM
63545-268Asarum EuropaeumAsarum Europaeum
63545-269Asarum EuropaeumAsarum Europaeum
63545-270Asarum EuropaeumAsarum Europaeum
63545-271Asarum EuropaeumAsarum Europaeum
63545-272Asarum EuropaeumAsarum Europaeum
63545-273Asarum EuropaeumAsarum Europaeum
63545-274Asarum EuropaeumAsarum Europaeum
68428-232Asarum europaeumASARUM EUROPAEUM
71919-092Asarum europaeumASARUM EUROPAEUM
64117-111Nervous HeadacheASARUM EUROPAEUM

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