Lithium Carbonate

Product NDC
50090-2799
11-digit product format
500902799
Labeler code
50090
Product ID
50090-2799_43321c58-edd9-4767-adae-c7fa07d5a16c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lithium Carbonate
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA017812
Marketing category
NDA
Marketing start
1980-11-26
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2799-0EA - Each50090-2799b0b9e37b-581d-4320-9580-530c7c35c9ea12018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-2799-05009027990032 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2799-0) > 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK32 blister pack2017-01-190000-00-00NoNoCurrent