NDC 37662-1907

Paeonia Officinalis

Paeonia Officinalis

Paeonia Officinalis is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Hahnemann Laboratories, Inc.. The primary component is Paeonia Officinalis Root.

Product ID37662-1907_ed03a980-af18-59d4-e053-2995a90a583e
NDC37662-1907
Product TypeHuman Otc Drug
Proprietary NamePaeonia Officinalis
Generic NamePaeonia Officinalis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2022-11-14
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameHahnemann Laboratories, INC.
Substance NamePAEONIA OFFICINALIS ROOT
Active Ingredient Strength100 [hp_C]/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 37662-1907-1

200 PELLET in 1 VIAL, GLASS (37662-1907-1)
Marketing Start Date2022-11-14
NDC Exclude FlagN
Sample Package?N

Drug Details

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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.