NDC 15631-0262

LACHNANTHES TINCTORIA

Lachnanthes Tinctoria

LACHNANTHES TINCTORIA 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 Lachnanthes Caroliniana.

Product ID15631-0262_a182a9d3-2b4b-d32b-e053-2995a90a6cdd
NDC15631-0262
Product TypeHuman Otc Drug
Proprietary NameLACHNANTHES TINCTORIA
Generic NameLachnanthes Tinctoria
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLACHNANTHES CAROLINIANA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0262-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0262-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0262-1 [15631026201]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0262-5 [15631026205]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0262-2 [15631026202]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0262-3 [15631026203]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0262-4 [15631026204]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0262-0 [15631026200]

LACHNANTHES TINCTORIA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
LACHNANTHES CAROLINIANA1 [hp_X]/1

OpenFDA Data

SPL SET ID:a54ee1ed-50ec-4e81-8330-e8537aaae0cf
Manufacturer
UNII

NDC Crossover Matching brand name "LACHNANTHES TINCTORIA" or generic name "Lachnanthes Tinctoria"

NDCBrand NameGeneric Name
0220-3033Lachnanthes tinctoriaLACHNANTHES CAROLINIANA
0220-3038Lachnanthes tinctoriaLACHNANTHES CAROLINIANA
0220-3039Lachnanthes tinctoriaLACHNANTHES CAROLINIANA
15631-0262LACHNANTHES TINCTORIALACHNANTHES TINCTORIA
68428-465Lachnanthes tinctoriaLACHNANTHES CAROLINIANA
71919-400Lachnanthes tinctoriaLACHNANTHES CAROLINIANA

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.