NDC 69152-1017

Ledum palustre 200C

Ledum Palustre

Ledum palustre 200C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Ledum Palustre Twig.

Product ID69152-1017_344c0897-3300-1fb6-e054-00144ff8d46c
NDC69152-1017
Product TypeHuman Otc Drug
Proprietary NameLedum palustre 200C
Generic NameLedum Palustre
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-08
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NameLEDUM PALUSTRE TWIG
Active Ingredient Strength200 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1017-1

96 PELLET in 1 BOTTLE (69152-1017-1)
Marketing Start Date2015-06-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1017-1 [69152101701]

Ledum palustre 200C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-08
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LEDUM PALUSTRE TWIG200 [hp_C]/1

OpenFDA Data

SPL SET ID:17fd8ca9-4ebf-5d77-e054-00144ff88e88
Manufacturer
UNII

NDC Crossover Matching brand name "Ledum palustre 200C" or generic name "Ledum Palustre"

NDCBrand NameGeneric Name
69152-1017Ledum palustre 200CLedum palustre
15631-0272LEDUM PALUSTRELEDUM PALUSTRE
15631-0624LEDUM PALUSTRELEDUM PALUSTRE
37662-1741Ledum PalustreLedum Palustre
37662-1742Ledum PalustreLedum Palustre
37662-1743Ledum PalustreLedum Palustre
37662-1744Ledum PalustreLedum Palustre
37662-1745Ledum PalustreLedum Palustre
37662-1746Ledum PalustreLedum Palustre
37662-1747Ledum PalustreLedum Palustre
37662-1748Ledum PalustreLedum Palustre
37662-1749Ledum PalustreLedum Palustre
53645-1541Ledum PalustreLedum Palustre
60512-6780LEDUM PALUSTRELEDUM PALUSTRE
63083-7125Ledum palustreLedum palustre
76472-3023Ledum PalustreLedum Palustre

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