NDC 15631-0041

APOCYNUM CANNABINUM

Apocynum Cannabinum

APOCYNUM CANNABINUM 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 Apocynum Cannabinum Root.

Product ID15631-0041_27a4822a-e97b-42e4-878e-6dac16764d59
NDC15631-0041
Product TypeHuman Otc Drug
Proprietary NameAPOCYNUM CANNABINUM
Generic NameApocynum Cannabinum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAPOCYNUM CANNABINUM ROOT
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0041-0

100 PELLET in 1 PACKAGE (15631-0041-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0041-1 [15631004101]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0041-5 [15631004105]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0041-3 [15631004103]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0041-4 [15631004104]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0041-2 [15631004102]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0041-0 [15631004100]

APOCYNUM CANNABINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

Drug Details

Active Ingredients

IngredientStrength
APOCYNUM CANNABINUM ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:649d743b-1bb7-4ea1-9566-36a90985cde6
Manufacturer
UNII

NDC Crossover Matching brand name "APOCYNUM CANNABINUM" or generic name "Apocynum Cannabinum"

NDCBrand NameGeneric Name
0220-0421Apocynum cannabinumAPOCYNUM CANNABINUM ROOT
0220-0428Apocynum cannabinumAPOCYNUM CANNABINUM ROOT
15631-0041APOCYNUM CANNABINUMAPOCYNUM CANNABINUM
15631-0516APOCYNUM CANNABINUMAPOCYNUM CANNABINUM
63545-058Apocynum CannabinumApocynum Cannabinum
63545-059Apocynum CannabinumApocynum Cannabinum
63545-060Apocynum CannabinumApocynum Cannabinum
63545-061Apocynum CannabinumApocynum Cannabinum
63545-062Apocynum CannabinumApocynum Cannabinum
63545-063Apocynum CannabinumApocynum Cannabinum
63545-064Apocynum CannabinumApocynum Cannabinum
63545-065Apocynum CannabinumApocynum Cannabinum
63545-066Apocynum CannabinumApocynum Cannabinum
68428-217Apocynum cannabinumAPOCYNUM CANNABINUM ROOT
71919-069Apocynum cannabinumAPOCYNUM CANNABINUM ROOT
69152-1555Apocynum cannabinum 1XApocynum cannabinum

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