Lithium Carbonate

Product NDC

70518-0360

11-digit product format

705180360

Labeler code

70518

Product ID

70518-0360_83d74b52-a1c9-5664-e053-2a91aa0a9bfd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lithium carbonate

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202288

Marketing category

ANDA

Marketing start

2017-03-23

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