Lithium Carbonate

Product NDC

70518-0150

11-digit product format

705180150

Labeler code

70518

Product ID

70518-0150_79023770-d71d-6d5d-e053-2a91aa0acece

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lithium Carbonate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018558

Marketing category

NDA

Marketing start

2017-01-19

Marketing end

0000-00-00

Substance

LITHIUM CARBONATE

Active strength

300 mg/1

Pharmacologic classes

Mood Stabilizer [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record