NDC 15631-0005

ACONITUM NAPELLUS

Aconitum Napellus

ACONITUM NAPELLUS 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 Aconitum Napellus.

Product ID15631-0005_1d407ada-266d-4d4c-86ac-25bb7634c860
NDC15631-0005
Product TypeHuman Otc Drug
Proprietary NameACONITUM NAPELLUS
Generic NameAconitum Napellus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameACONITUM NAPELLUS
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0005-0

100 PELLET in 1 PACKAGE (15631-0005-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0005-3 [15631000503]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0005-2 [15631000502]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0005-5 [15631000505]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0005-1 [15631000501]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0005-0 [15631000500]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0005-4 [15631000504]

ACONITUM NAPELLUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS3 [hp_X]/1

OpenFDA Data

SPL SET ID:eace2915-a54b-4649-9bd0-19461ff28dd5
Manufacturer
UNII

NDC Crossover Matching brand name "ACONITUM NAPELLUS" or generic name "Aconitum Napellus"

NDCBrand NameGeneric Name
0220-0027Aconitum napellusACONITUM NAPELLUS
0220-0028Aconitum napellusACONITUM NAPELLUS
0220-0031Aconitum napellusACONITUM NAPELLUS
0220-0032Aconitum napellusACONITUM NAPELLUS
0220-0035Aconitum napellusACONITUM NAPELLUS
0220-0036Aconitum napellusACONITUM NAPELLUS
0220-0039Aconitum napellusACONITUM NAPELLUS
0220-0040Aconitum napellusACONITUM NAPELLUS
0220-0043Aconitum napellusACONITUM NAPELLUS
0220-0045Aconitum napellusACONITUM NAPELLUS
0220-0050Aconitum napellusACONITUM NAPELLUS
0220-0052Aconitum napellusACONITUM NAPELLUS
15631-0005ACONITUM NAPELLUSACONITUM NAPELLUS
15631-0502ACONITUM NAPELLUSACONITUM NAPELLUS
57556-010Aconitum napellusAconite
60512-1001ACONITUM NAPELLUSACONITUM NAPELLUS
62106-7197ACONITUM NAPELLUSAconite
63083-7101Aconitum napellusAconitum napellus
63545-144Aconitum napellusAconitum napellus
68428-177Aconitum napellusAconitum napellus
71919-009Aconitum napellusAconitum napellus
76472-1123ACONITUM NAPELLUSACONITUM NAPELLUS
66096-777Aconitum NapellusAconitum Napellus
63545-736Aconitum napellusAconitum napellus
63545-737Aconitum napellusAconitum napellus
63545-738Aconitum napellusAconitum napellus
63545-733Aconitum napellusAconitum napellus
63545-732Aconitum napellusAconitum napellus
63545-735Aconitum napellusAconitum napellus
63545-734Aconitum napellusAconitum napellus
44911-0152AconiteAconitum Napellus
44911-0209ACONITEAconitum napellus
0360-0005ACONITUMACONITUM NAPELLUS
43406-0159Aconitum Napellus 200CAconitum Napellus
55714-9009Arnica montanaAconitum napellus

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