Lithium Carbonate

Product NDC

70518-0629

11-digit product format

705180629

Labeler code

70518

Product ID

70518-0629_86455058-2734-5c0a-e053-2a91aa0ac659

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lithium Carbonate Extended-Release Tablet

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018027

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2017-07-19

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

2020-12-31

Current FDA listing

Historical FDA.report record