NDC 15631-0326

PAEONIA OFFICINALIS

Paeonia Officinalis

PAEONIA 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 Paeonia Officinalis Root.

Product ID15631-0326_11c05266-39b5-4584-a40b-2590505dc971
NDC15631-0326
Product TypeHuman Otc Drug
Proprietary NamePAEONIA OFFICINALIS
Generic NamePaeonia Officinalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePAEONIA OFFICINALIS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0326-0

100 PELLET in 1 PACKAGE (15631-0326-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0326-1 [15631032601]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0326-0 [15631032600]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0326-2 [15631032602]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0326-5 [15631032605]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0326-3 [15631032603]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0326-4 [15631032604]

PAEONIA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
PAEONIA OFFICINALIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:a99d0bed-22ea-4141-ba6c-962a9eafeb45
Manufacturer
UNII

NDC Crossover Matching brand name "PAEONIA OFFICINALIS" or generic name "Paeonia Officinalis"

NDCBrand NameGeneric Name
0220-3900Paeonia officinalisPAEONIA OFFICINALIS ROOT
0220-3901Paeonia officinalisPAEONIA OFFICINALIS ROOT
15631-0326PAEONIA OFFICINALISPAEONIA OFFICINALIS
15631-0646PAEONIA OFFICINALISPAEONIA OFFICINALIS
37662-1904Paeonia OfficinalisPaeonia Officinalis
37662-1905Paeonia OfficinalisPaeonia Officinalis
37662-1906Paeonia OfficinalisPaeonia Officinalis
37662-1907Paeonia OfficinalisPaeonia Officinalis
37662-1908Paeonia OfficinalisPaeonia Officinalis
37662-1909Paeonia OfficinalisPaeonia Officinalis
37662-1910Paeonia OfficinalisPaeonia Officinalis
68428-550Paeonia officinalisPAEONIA OFFICINALIS ROOT
71919-516Paeonia officinalisPAEONIA OFFICINALIS ROOT

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