Lithium - 60986-1019-4 - (Lithium Bromatum)

Alphabetical Index


Drug Information of Lithium

Product NDC: 60986-1019
Proprietary Name: Lithium
Non Proprietary Name: Lithium Bromatum
Active Ingredient(s): 3    [hp_X]/mL & nbsp;   Lithium Bromatum
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium

Product NDC: 60986-1019
Labeler Name: Marco Pharma International LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19920301

Package Information of Lithium

Package NDC: 60986-1019-4
Package Description: 100 mL in 1 BOTTLE, GLASS (60986-1019-4)

NDC Information of Lithium

NDC Code 60986-1019-4
Proprietary Name Lithium
Package Description 100 mL in 1 BOTTLE, GLASS (60986-1019-4)
Product NDC 60986-1019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lithium Bromatum
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19920301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Marco Pharma International LLC.
Substance Name LITHIUM BROMIDE
Strength Number 3
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Lithium


General Information