NDC 15631-0366

RATANHIA

Ratanhia

RATANHIA 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 Krameria Lappacea Root.

Product ID15631-0366_a1bd4b93-3b91-56cf-e053-2995a90a981a
NDC15631-0366
Product TypeHuman Otc Drug
Proprietary NameRATANHIA
Generic NameRatanhia
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameKRAMERIA LAPPACEA ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0366-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0366-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0366-3 [15631036603]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0366-0 [15631036600]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0366-2 [15631036602]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0366-4 [15631036604]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0366-5 [15631036605]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0366-1 [15631036601]

RATANHIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
KRAMERIA LAPPACEA ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:5958ede9-618f-4508-8f60-b11eba6abd77
Manufacturer
UNII

NDC Crossover Matching brand name "RATANHIA" or generic name "Ratanhia"

NDCBrand NameGeneric Name
0220-4337RatanhiaKRAMERIA LAPPACEA ROOT
0220-4338RatanhiaKRAMERIA LAPPACEA ROOT
0220-4339RatanhiaKRAMERIA LAPPACEA ROOT
15631-0366RATANHIARATANHIA
37662-1404RatanhiaRatanhia
37662-1405RatanhiaRatanhia
37662-1406RatanhiaRatanhia
37662-1407RatanhiaRatanhia
37662-1408RatanhiaRatanhia
37662-1409RatanhiaRatanhia
37662-1410RatanhiaRatanhia
37662-1411RatanhiaRatanhia
68428-596RatanhiaKRAMERIA LAPPACEA ROOT
71919-575RatanhiaKRAMERIA LAPPACEA ROOT
69152-1060Ratanhia 200CRatanhia

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