NDC 15631-0319

OLEANDER

Oleander

OLEANDER 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 Nerium Oleander Leaf.

Product ID15631-0319_a199cdd9-69ac-9316-e053-2a95a90a3f89
NDC15631-0319
Product TypeHuman Otc Drug
Proprietary NameOLEANDER
Generic NameOleander
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameNERIUM OLEANDER LEAF
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0319-0

100 PELLET in 1 PACKAGE (15631-0319-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0319-1 [15631031901]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0319-3 [15631031903]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0319-5 [15631031905]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0319-2 [15631031902]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0319-4 [15631031904]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0319-0 [15631031900]

OLEANDER PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
NERIUM OLEANDER LEAF3 [hp_X]/1

OpenFDA Data

SPL SET ID:c9c84acb-8c56-4642-898a-8c34b5eea40a
Manufacturer
UNII

NDC Crossover Matching brand name "OLEANDER" or generic name "Oleander"

NDCBrand NameGeneric Name
0220-3757OleanderNERIUM OLEANDER LEAF
0220-3760OleanderNERIUM OLEANDER LEAF
15631-0319OLEANDEROLEANDER
37662-1985OleanderOleander
37662-1986OleanderOleander
37662-1987OleanderOleander
37662-1988OleanderOleander
37662-1989OleanderOleander
37662-1990OleanderOleander
37662-1991OleanderOleander
68428-539OleanderNERIUM OLEANDER LEAF
71919-502OleanderNERIUM OLEANDER LEAF

Trademark Results [OLEANDER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OLEANDER
OLEANDER
88243454 not registered Live/Pending
HUANG JIAXIN
2018-12-27
OLEANDER
OLEANDER
88238118 not registered Dead/Abandoned
HUANG JIAXIN
2018-12-21
OLEANDER
OLEANDER
88073903 not registered Live/Pending
Misig Inc.
2018-08-10
OLEANDER
OLEANDER
87118870 5312892 Live/Registered
Wildeflower, LLC
2016-07-27
OLEANDER
OLEANDER
85303470 not registered Dead/Abandoned
Nerium Biotechnology, Inc.
2011-04-25
OLEANDER
OLEANDER
75881129 2425041 Dead/Cancelled
Oleander
1999-12-27
OLEANDER
OLEANDER
75881128 2402195 Dead/Cancelled
Oleander
1999-12-27
OLEANDER
OLEANDER
74136184 1735710 Dead/Cancelled
OHIO MATTRESS COMPANY LICENSING AND COMPONENTS GROUP, THE
1991-02-04

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