Lithium - 55154-4952-5 - (Lithium Carbonate)

Alphabetical Index


Drug Information of Lithium

Product NDC: 55154-4952
Proprietary Name: Lithium
Non Proprietary Name: Lithium Carbonate
Active Ingredient(s): 8    meq/5mL & nbsp;   Lithium Carbonate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lithium

Product NDC: 55154-4952
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018421
Marketing Category: NDA
Start Marketing Date: 19820429

Package Information of Lithium

Package NDC: 55154-4952-5
Package Description: 5 CUP, UNIT-DOSE in 1 BAG (55154-4952-5) > 5 mL in 1 CUP, UNIT-DOSE

NDC Information of Lithium

NDC Code 55154-4952-5
Proprietary Name Lithium
Package Description 5 CUP, UNIT-DOSE in 1 BAG (55154-4952-5) > 5 mL in 1 CUP, UNIT-DOSE
Product NDC 55154-4952
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lithium Carbonate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19820429
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name LITHIUM CARBONATE
Strength Number 8
Strength Unit meq/5mL
Pharmaceutical Classes Mood Stabilizer [EPC]

Complete Information of Lithium


General Information