NDC 15631-0394

SCROPHULARIA NODOSA

Scrophularia Nodosa

SCROPHULARIA NODOSA 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 Scrophularia Nodosa.

Product ID15631-0394_a1c1850f-2fed-fde0-e053-2995a90a6dde
NDC15631-0394
Product TypeHuman Otc Drug
Proprietary NameSCROPHULARIA NODOSA
Generic NameScrophularia Nodosa
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 NameSCROPHULARIA NODOSA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0394-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0394-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0394-0 [15631039400]

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

NDC 15631-0394-5 [15631039405]

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

NDC 15631-0394-2 [15631039402]

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

NDC 15631-0394-4 [15631039404]

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

NDC 15631-0394-1 [15631039401]

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

NDC 15631-0394-3 [15631039403]

SCROPHULARIA NODOSA 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
SCROPHULARIA NODOSA1 [hp_X]/1

OpenFDA Data

SPL SET ID:7bc3b9d5-1a22-41f3-a998-a9b0326c945a
Manufacturer
UNII

NDC Crossover Matching brand name "SCROPHULARIA NODOSA" or generic name "Scrophularia Nodosa"

NDCBrand NameGeneric Name
0220-4606Scrophularia nodosaSCROPHULARIA NODOSA
0220-4607Scrophularia nodosaSCROPHULARIA NODOSA
15631-0394SCROPHULARIA NODOSASCROPHULARIA NODOSA
37662-1223Scrophularia NodosaScrophularia Nodosa
37662-1224Scrophularia NodosaScrophularia Nodosa
37662-1225Scrophularia NodosaScrophularia Nodosa
37662-1226Scrophularia NodosaScrophularia Nodosa
37662-1227Scrophularia NodosaScrophularia Nodosa
37662-1228Scrophularia NodosaScrophularia Nodosa
37662-1229Scrophularia NodosaScrophularia Nodosa
37662-1230Scrophularia NodosaScrophularia Nodosa
68428-627Scrophularia nodosaSCROPHULARIA NODOSA
71919-616Scrophularia nodosaSCROPHULARIA NODOSA
64117-180HemmorrhoidsSCROPHULARIA NODOSA

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