NDC 15631-0379

RUTA GRAVEOLENS

Ruta Graveolens

RUTA GRAVEOLENS 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 Ruta Graveolens Flowering Top.

Product ID15631-0379_613b8fe4-b5e2-4d5f-ab56-aa13c2994233
NDC15631-0379
Product TypeHuman Otc Drug
Proprietary NameRUTA GRAVEOLENS
Generic NameRuta Graveolens
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameRUTA GRAVEOLENS FLOWERING TOP
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0379-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0379-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0379-0 [15631037900]

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

NDC 15631-0379-2 [15631037902]

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

NDC 15631-0379-1 [15631037901]

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

NDC 15631-0379-3 [15631037903]

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

NDC 15631-0379-5 [15631037905]

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

NDC 15631-0379-4 [15631037904]

RUTA GRAVEOLENS 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
RUTA GRAVEOLENS FLOWERING TOP1 [hp_X]/1

OpenFDA Data

SPL SET ID:f22fbf78-1ad9-4dbf-be49-b4043927d5e3
Manufacturer
UNII

NDC Crossover Matching brand name "RUTA GRAVEOLENS" or generic name "Ruta Graveolens"

NDCBrand NameGeneric Name
0220-4443Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4462Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4463Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4464Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4465Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4466Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4467Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4468Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4469Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0220-4470Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
0360-0332RUTA GRAVEOLENSRUTA GRAV
0360-0333RUTA GRAVEOLENSRUTA GRAV
15631-0379RUTA GRAVEOLENSRUTA GRAVEOLENS
15631-0673RUTA GRAVEOLENSRUTA GRAVEOLENS
37662-2261Ruta GraveolensRuta Graveolens
37662-2262Ruta GraveolensRuta Graveolens
37662-2263Ruta GraveolensRuta Graveolens
37662-2264Ruta GraveolensRuta Graveolens
37662-2265Ruta GraveolensRuta Graveolens
37662-2266Ruta GraveolensRuta Graveolens
37662-2267Ruta GraveolensRuta Graveolens
37662-2268Ruta GraveolensRuta Graveolens
37662-2269Ruta GraveolensRuta Graveolens
60512-1041RUTA GRAVEOLENSRUTA GRAVEOLENS
62106-8810RUTA GRAVEOLENSRue
63083-7133Ruta graveolensRuta graveolens
68428-609Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
71919-595Ruta graveolensRUTA GRAVEOLENS FLOWERING TOP
76472-1160Ruta GraveolensRUTA GRAVEOLENS
76472-3032RUTA GRAVEOLENSRUTA GRAVEOLENS
76029-001Pain ReliefRuta Graveolens
69152-1098Ruta graveolens 200CRuta graveolens
69152-1174Ruta graveolens 6CRuta graveolens
76472-4032Ruta Graveolens 6CRUTA GRAVEOLENS
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