NDC 15631-0270

LAUROCERASUS

Laurocerasus

LAUROCERASUS 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 Prunus Laurocerasus Leaf.

Product ID15631-0270_9935f9a0-fed2-424c-b86b-160353b3c0de
NDC15631-0270
Product TypeHuman Otc Drug
Proprietary NameLAUROCERASUS
Generic NameLaurocerasus
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 NamePRUNUS LAUROCERASUS LEAF
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0270-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0270-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0270-1 [15631027001]

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

NDC 15631-0270-2 [15631027002]

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

NDC 15631-0270-4 [15631027004]

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

NDC 15631-0270-5 [15631027005]

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

NDC 15631-0270-0 [15631027000]

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

NDC 15631-0270-3 [15631027003]

LAUROCERASUS 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
PRUNUS LAUROCERASUS LEAF3 [hp_X]/1

OpenFDA Data

SPL SET ID:19636e15-0d8b-4d89-85d2-f0be1f3a03c1
Manufacturer
UNII

NDC Crossover Matching brand name "LAUROCERASUS" or generic name "Laurocerasus"

NDCBrand NameGeneric Name
0220-3069LaurocerasusPRUNUS LAUROCERASUS LEAF
15631-0270LAUROCERASUSLAUROCERASUS
37662-1750LaurocerasusLaurocerasus
37662-1751LaurocerasusLaurocerasus
37662-1752LaurocerasusLaurocerasus
37662-1753LaurocerasusLaurocerasus
37662-1754LaurocerasusLaurocerasus
37662-1755LaurocerasusLaurocerasus
37662-1756LaurocerasusLaurocerasus
37662-1757LaurocerasusLaurocerasus
37662-1758LaurocerasusLaurocerasus
68428-970LaurocerasusPRUNUS LAUROCERASUS LEAF
71919-407LaurocerasusPRUNUS LAUROCERASUS LEAF

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