NDC 15631-0453

VALERIANA OFFICINALIS

Valeriana Officinalis

VALERIANA OFFICINALIS 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 Valerian.

Product ID15631-0453_a1d304f3-07b9-77b5-e053-2995a90a0e81
NDC15631-0453
Product TypeHuman Otc Drug
Proprietary NameVALERIANA OFFICINALIS
Generic NameValeriana Officinalis
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 NameVALERIAN
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0453-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0453-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0453-2 [15631045302]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0453-0 [15631045300]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0453-1 [15631045301]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0453-3 [15631045303]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0453-5 [15631045305]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0453-4 [15631045304]

VALERIANA OFFICINALIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
VALERIAN1 [hp_X]/1

OpenFDA Data

SPL SET ID:5f4ecb75-12df-4819-8ddb-198d9da0a075
Manufacturer
UNII

NDC Crossover Matching brand name "VALERIANA OFFICINALIS" or generic name "Valeriana Officinalis"

NDCBrand NameGeneric Name
0220-5207VALERIANA OFFICINALISVALERIAN
0220-5208VALERIANA OFFICINALISVALERIAN
0220-5209VALERIANA OFFICINALISVALERIAN
0220-5210VALERIANA OFFICINALISVALERIAN
0220-5217Valeriana officinalisVALERIAN
0360-0387VALERIANA OFFICINALISVALERIANA OFF
0360-0388VALERIANA OFFICINALISVALERIANA OFF
15631-0453VALERIANA OFFICINALISVALERIANA OFFICINALIS
62106-9130VALERIANA OFFICINALISValerian
68428-693Valeriana OfficinalisVALERIAN
71919-702VALERIANA OFFICINALISValerian

© 2022 FDA.report
This site is not affiliated with or endorsed by the FDA.