NDC 15631-0211

GRATIOLA OFFICINALIS

Gratiola Officinalis

GRATIOLA 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 Gratiola Officinalis.

Product ID15631-0211_00302efb-4622-4a50-a437-cc8cfe0b81aa
NDC15631-0211
Product TypeHuman Otc Drug
Proprietary NameGRATIOLA OFFICINALIS
Generic NameGratiola Officinalis
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 NameGRATIOLA OFFICINALIS
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0211-0

100 PELLET in 1 PACKAGE (15631-0211-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0211-1 [15631021101]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0211-2 [15631021102]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0211-3 [15631021103]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0211-5 [15631021105]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0211-0 [15631021100]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0211-4 [15631021104]

GRATIOLA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
GRATIOLA OFFICINALIS1 [hp_X]/1

OpenFDA Data

SPL SET ID:5c9ca995-e068-49da-9aad-6090cb53a599
Manufacturer
UNII

NDC Crossover Matching brand name "GRATIOLA OFFICINALIS" or generic name "Gratiola Officinalis"

NDCBrand NameGeneric Name
0220-2329Gratiola officinalisGRATIOLA OFFICINALIS
15631-0211GRATIOLA OFFICINALISGRATIOLA OFFICINALIS
68428-947Gratiola officinalisGRATIOLA OFFICINALIS
71919-325Gratiola officinalisGRATIOLA OFFICINALIS
64117-234STOMACH CRAMPSGRATIOLA OFFICINALIS

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