NDC 15631-0276

LITHIUM CARBONICUM

Lithium Carbonicum

LITHIUM CARBONICUM 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 Lithium Carbonate.

Product ID15631-0276_a185c59d-5782-0403-e053-2a95a90a58cd
NDC15631-0276
Product TypeHuman Otc Drug
Proprietary NameLITHIUM CARBONICUM
Generic NameLithium Carbonicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameLITHIUM CARBONATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0276-0

100 PELLET in 1 PACKAGE (15631-0276-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0276-1 [15631027601]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0276-0 [15631027600]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0276-2 [15631027602]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0276-4 [15631027604]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0276-3 [15631027603]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0276-5 [15631027605]

LITHIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
LITHIUM CARBONATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:a376845b-944b-4c7e-a4fa-f64a46169af7
Manufacturer
UNII

NDC Crossover Matching brand name "LITHIUM CARBONICUM" or generic name "Lithium Carbonicum"

NDCBrand NameGeneric Name
0220-3128Lithium carbonicumLITHIUM CARBONATE
0220-3131Lithium carbonicumLITHIUM CARBONATE
15631-0276LITHIUM CARBONICUMLITHIUM CARBONICUM
37662-0935Lithium CarbonicumLithium Carbonicum
37662-0936Lithium CarbonicumLithium Carbonicum
37662-0937Lithium CarbonicumLithium Carbonicum
37662-0938Lithium CarbonicumLithium Carbonicum
37662-0939Lithium CarbonicumLithium Carbonicum
37662-0940Lithium CarbonicumLithium Carbonicum
37662-0941Lithium CarbonicumLithium Carbonicum
68428-481Lithium carbonicumLITHIUM CARBONATE
71919-421Lithium carbonicumLITHIUM CARBONATE
44911-0147Lithium CarbLithium Carbonicum

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