NDC 15631-0248

KALI BROMATUM

Kali Bromatum

KALI BROMATUM 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 Potassium Bromide.

Product ID15631-0248_8cd4a8c5-41a9-4c4d-a02b-008080536393
NDC15631-0248
Product TypeHuman Otc Drug
Proprietary NameKALI BROMATUM
Generic NameKali Bromatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePOTASSIUM BROMIDE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0248-0

100 PELLET in 1 PACKAGE (15631-0248-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0248-5 [15631024805]

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

NDC 15631-0248-0 [15631024800]

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

NDC 15631-0248-3 [15631024803]

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

NDC 15631-0248-2 [15631024802]

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

NDC 15631-0248-4 [15631024804]

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

NDC 15631-0248-1 [15631024801]

KALI BROMATUM 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
POTASSIUM BROMIDE1 [hp_X]/1

OpenFDA Data

SPL SET ID:04572087-c0c2-4ed9-8836-a159a62f1bf4
Manufacturer
UNII

NDC Crossover Matching brand name "KALI BROMATUM" or generic name "Kali Bromatum"

NDCBrand NameGeneric Name
0220-2819Kali bromatumPOTASSIUM BROMIDE
0220-2820Kali bromatumPOTASSIUM BROMIDE
0220-2821Kali bromatumPOTASSIUM BROMIDE
0220-2822Kali bromatumPOTASSIUM BROMIDE
0220-2823Kali bromatumPOTASSIUM BROMIDE
0220-2824Kali bromatumPOTASSIUM BROMIDE
0220-2859Kali bromatumPOTASSIUM BROMIDE
15631-0248KALI BROMATUMKALI BROMATUM
37662-0867Kali BromatumKali Bromatum
37662-0868Kali BromatumKali Bromatum
37662-0869Kali BromatumKali Bromatum
37662-0870Kali BromatumKali Bromatum
37662-0871Kali BromatumKali Bromatum
37662-0872Kali BromatumKali Bromatum
37662-0873Kali BromatumKali Bromatum
37662-0874Kali BromatumKali Bromatum
68428-450Kali bromatumPOTASSIUM BROMIDE
71919-379Kali bromatumPOTASSIUM BROMIDE

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