NDC 15631-0061

ASPARAGUS OFFICINALIS

Asparagus Officinalis

ASPARAGUS OFFICINALIS 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 Asparagus.

Product ID15631-0061_9ec83fde-8670-1868-e053-2995a90a9842
NDC15631-0061
Product TypeHuman Otc Drug
Proprietary NameASPARAGUS OFFICINALIS
Generic NameAsparagus Officinalis
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 NameASPARAGUS
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0061-0

100 PELLET in 1 PACKAGE (15631-0061-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0061-0 [15631006100]

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

NDC 15631-0061-3 [15631006103]

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

NDC 15631-0061-1 [15631006101]

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

NDC 15631-0061-2 [15631006102]

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

NDC 15631-0061-5 [15631006105]

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

NDC 15631-0061-4 [15631006104]

ASPARAGUS OFFICINALIS 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
ASPARAGUS2 [hp_X]/1

OpenFDA Data

SPL SET ID:d7bd9d3c-91a7-4089-8c7e-8e171b480318
Manufacturer
UNII

NDC Crossover Matching brand name "ASPARAGUS OFFICINALIS" or generic name "Asparagus Officinalis"

NDCBrand NameGeneric Name
15631-0061ASPARAGUS OFFICINALISASPARAGUS OFFICINALIS
63545-275Asparagus OfficinalisAsparagus Officinalis
63545-276Asparagus OfficinalisAsparagus Officinalis
63545-277Asparagus OfficinalisAsparagus Officinalis
63545-278Asparagus OfficinalisAsparagus Officinalis
63545-279Asparagus OfficinalisAsparagus Officinalis
63545-280Asparagus OfficinalisAsparagus Officinalis
63545-281Asparagus OfficinalisAsparagus Officinalis
68428-234Asparagus officinalisASPARAGUS
71919-094Asparagus officinalisASPARAGUS
0268-6103ASPARAGUSASPARAGUS OFFICINALIS

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