NDC 15631-0266

LAPIS ALBUS

Lapis Albus

LAPIS ALBUS 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 Calcium Hexafluorosilicate.

Product ID15631-0266_952d4ac3-98e4-4010-8435-ac1bdb8a1d19
NDC15631-0266
Product TypeHuman Otc Drug
Proprietary NameLAPIS ALBUS
Generic NameLapis Albus
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 NameCALCIUM HEXAFLUOROSILICATE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0266-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0266-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0266-5 [15631026605]

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

NDC 15631-0266-1 [15631026601]

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

NDC 15631-0266-2 [15631026602]

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

NDC 15631-0266-4 [15631026604]

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

NDC 15631-0266-0 [15631026600]

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

NDC 15631-0266-3 [15631026603]

LAPIS ALBUS 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
CALCIUM HEXAFLUOROSILICATE6 [hp_X]/1

OpenFDA Data

SPL SET ID:b837fff3-4771-4a3e-8428-8eb48e7fe673
Manufacturer
UNII

NDC Crossover Matching brand name "LAPIS ALBUS" or generic name "Lapis Albus"

NDCBrand NameGeneric Name
0220-3053Lapis albusCALCIUM HEXAFLUOROSILICATE
0220-3055Lapis albusCALCIUM HEXAFLUOROSILICATE
15631-0266LAPIS ALBUSLAPIS ALBUS
68428-468Lapis albusCALCIUM HEXAFLUOROSILICATE
71919-403Lapis albusCALCIUM HEXAFLUOROSILICATE

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