NDC 15631-0395

SCUTELLARIA LATERIFLORA

Scutellaria Lateriflora

SCUTELLARIA LATERIFLORA 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 Scutellaria Lateriflora.

Product ID15631-0395_a1c18ed2-6357-352c-e053-2995a90ae027
NDC15631-0395
Product TypeHuman Otc Drug
Proprietary NameSCUTELLARIA LATERIFLORA
Generic NameScutellaria Lateriflora
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 NameSCUTELLARIA LATERIFLORA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0395-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0395-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0395-2 [15631039502]

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

NDC 15631-0395-4 [15631039504]

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

NDC 15631-0395-5 [15631039505]

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

NDC 15631-0395-1 [15631039501]

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

NDC 15631-0395-3 [15631039503]

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

NDC 15631-0395-0 [15631039500]

SCUTELLARIA LATERIFLORA 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
SCUTELLARIA LATERIFLORA1 [hp_X]/1

OpenFDA Data

SPL SET ID:09584000-07a4-4fba-823f-3608e5f717b9
Manufacturer
UNII

NDC Crossover Matching brand name "SCUTELLARIA LATERIFLORA" or generic name "Scutellaria Lateriflora"

NDCBrand NameGeneric Name
0220-4610Scutellaria laterifloraSCUTELLARIA LATERIFLORA
0220-4611Scutellaria laterifloraSCUTELLARIA LATERIFLORA
15631-0395SCUTELLARIA LATERIFLORASCUTELLARIA LATERIFLORA
37662-2270Scutellaria LaterifloraScutellaria Lateriflora
37662-2271Scutellaria LaterifloraScutellaria Lateriflora
37662-2272Scutellaria LaterifloraScutellaria Lateriflora
37662-2273Scutellaria LaterifloraScutellaria Lateriflora
37662-2274Scutellaria LaterifloraScutellaria Lateriflora
37662-2275Scutellaria LaterifloraScutellaria Lateriflora
37662-2276Scutellaria LaterifloraScutellaria Lateriflora
37662-2277Scutellaria LaterifloraScutellaria Lateriflora
37662-2278Scutellaria LaterifloraScutellaria Lateriflora
68428-628Scutellaria laterifloraSCUTELLARIA LATERIFLORA
71919-617Scutellaria laterifloraSCUTELLARIA LATERIFLORA

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