NDC 15631-0444

TILIA EUROPAEA

Tilia Europaea

TILIA EUROPAEA 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 Tilia X Europaea Flower.

Product ID15631-0444_a1d2e350-aad4-5253-e053-2a95a90a825b
NDC15631-0444
Product TypeHuman Otc Drug
Proprietary NameTILIA EUROPAEA
Generic NameTilia Europaea
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 NameTILIA X EUROPAEA FLOWER
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0444-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0444-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0444-5 [15631044405]

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

NDC 15631-0444-4 [15631044404]

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

NDC 15631-0444-1 [15631044401]

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

NDC 15631-0444-2 [15631044402]

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

NDC 15631-0444-0 [15631044400]

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

NDC 15631-0444-3 [15631044403]

TILIA EUROPAEA 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
TILIA X EUROPAEA FLOWER1 [hp_X]/1

OpenFDA Data

SPL SET ID:372741eb-9614-482f-b37b-d342cdf19f1d
Manufacturer
UNII

NDC Crossover Matching brand name "TILIA EUROPAEA" or generic name "Tilia Europaea"

NDCBrand NameGeneric Name
15631-0444TILIA EUROPAEATILIA EUROPAEA
68428-680Tilia europaeaTILIA X EUROPAEA FLOWER
71919-682TILIA EUROPAEATilia x europaea
44911-0221LINDEN FLOWER TINCTilia europaea

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