NDC 15631-0383

SACCHARUM LACTIS

Saccharum Lactis

SACCHARUM LACTIS 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 Lactose, Unspecified Form.

Product ID15631-0383_45d63067-26e1-4b19-aced-a6e43f4e9e88
NDC15631-0383
Product TypeHuman Otc Drug
Proprietary NameSACCHARUM LACTIS
Generic NameSaccharum Lactis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLACTOSE, UNSPECIFIED FORM
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0383-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0383-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0383-5 [15631038305]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0383-3 [15631038303]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0383-1 [15631038301]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0383-2 [15631038302]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0383-4 [15631038304]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0383-0 [15631038300]

SACCHARUM LACTIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
LACTOSE, UNSPECIFIED FORM1 [hp_X]/1

OpenFDA Data

SPL SET ID:a4f49264-1dda-4a37-b8e6-13e581730875
Manufacturer
UNII

NDC Crossover Matching brand name "SACCHARUM LACTIS" or generic name "Saccharum Lactis"

NDCBrand NameGeneric Name
15631-0383SACCHARUM LACTISSACCHARUM LACTIS
37662-1412Saccharum LactisSaccharum Lactis
37662-1413Saccharum LactisSaccharum Lactis
37662-1414Saccharum LactisSaccharum Lactis
37662-1415Saccharum LactisSaccharum Lactis
37662-1416Saccharum LactisSaccharum Lactis
37662-1417Saccharum LactisSaccharum Lactis
37662-1418Saccharum LactisSaccharum Lactis
37662-1419Saccharum LactisSaccharum Lactis
71919-600Saccharum lactisLACTOSE, UNSPECIFIED FORM

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