NDC 15631-0132

CHOLESTERINUM

Cholesterinum

CHOLESTERINUM 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 Cholesterol.

Product ID15631-0132_a0bf1728-76be-6ba9-e053-2a95a90ad24e
NDC15631-0132
Product TypeHuman Otc Drug
Proprietary NameCHOLESTERINUM
Generic NameCholesterinum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCHOLESTEROL
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0132-0

100 PELLET in 1 PACKAGE (15631-0132-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0132-0 [15631013200]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0132-4 [15631013204]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0132-1 [15631013201]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0132-5 [15631013205]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0132-3 [15631013203]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0132-2 [15631013202]

CHOLESTERINUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

Drug Details

Active Ingredients

IngredientStrength
CHOLESTEROL3 [hp_X]/1

OpenFDA Data

SPL SET ID:4b8e6dee-c718-47be-8593-144766c9153f
Manufacturer
UNII

NDC Crossover Matching brand name "CHOLESTERINUM" or generic name "Cholesterinum"

NDCBrand NameGeneric Name
0220-1334CholesterinumCHOLESTEROL
0220-1335CholesterinumCHOLESTEROL
0220-1339CholesterinumCHOLESTEROL
0220-1341CholesterinumCHOLESTEROL
15631-0132CHOLESTERINUMCHOLESTERINUM
62106-5732CHOLESTERINUMCholesterine
68428-315CholesterinumCHOLESTEROL
71919-194CholesterinumCHOLESTEROL
43742-0562CHOLESTEROLCholesterinum
43742-1272CholesterolCholesterinum

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.