NDC 15631-0646

PAEONIA OFFICINALIS

Paeonia Officinalis

PAEONIA OFFICINALIS is a Oral Tablet 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 ID15631-0646_274ba61a-a70b-4043-9899-9c92ea467ed9
NDC15631-0646
Product TypeHuman Otc Drug
Proprietary NamePAEONIA OFFICINALIS
Generic NamePaeonia Officinalis
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-26
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 15631-0646-3

100 TABLET in 1 CONTAINER (15631-0646-3)
Marketing Start Date2015-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0646-4 [15631064604]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-6 [15631064606]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-3 [15631064603]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-5 [15631064605]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-0 [15631064600]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-7 [15631064607]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-1 [15631064601]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0646-2 [15631064602]

PAEONIA OFFICINALIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PAEONIA OFFICINALIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:65f4f0ef-863d-454e-b46f-a57baf124b7a
Manufacturer
UNII
UPC Code
  • 8907460005526

    • 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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