Lithium Carbonate

Product NDC

53808-0884

11-digit product format

538080884

Labeler code

53808

Product ID

53808-0884_9d1794d1-822d-4ca7-9cad-6582a965df9a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lithium Carbonate

Dosage form

CAPSULE

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA079139

Marketing category

ANDA

Marketing start

2014-01-01

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