NDC 15631-0368

RHAMNUS FRANGULA

Rhamnus Frangula

RHAMNUS FRANGULA 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 Frangula Alnus Bark.

Product ID15631-0368_9b0545dd-3e40-420a-a21e-7d8e1febd4be
NDC15631-0368
Product TypeHuman Otc Drug
Proprietary NameRHAMNUS FRANGULA
Generic NameRhamnus Frangula
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 NameFRANGULA ALNUS BARK
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0368-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0368-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0368-3 [15631036803]

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

NDC 15631-0368-0 [15631036800]

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

NDC 15631-0368-1 [15631036801]

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

NDC 15631-0368-5 [15631036805]

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

NDC 15631-0368-4 [15631036804]

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

NDC 15631-0368-2 [15631036802]

RHAMNUS FRANGULA 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
FRANGULA ALNUS BARK2 [hp_X]/1

OpenFDA Data

SPL SET ID:dee8596f-4c22-4b29-9a33-cc002479ebf0
Manufacturer
UNII

NDC Crossover Matching brand name "RHAMNUS FRANGULA" or generic name "Rhamnus Frangula"

NDCBrand NameGeneric Name
15631-0368RHAMNUS FRANGULARHAMNUS FRANGULA
68428-598Rhamnus frangulaFRANGULA ALNUS BARK
71919-577Rhamnus frangulaFRANGULA ALNUS BARK

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