NDC 23155-763 – Lithium carbonate

Lithium Carbonate 300 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC23155-763

Product details

Brand name
Lithium carbonate
Generic name
Lithium carbonate
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205532
Marketed since
October 20, 2020
Listing expires
December 31, 2026
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Lithium Carbonate →

Package NDC codes (2)

Package NDCDescriptionSince
23155-763-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)Oct 20, 2020
23155-763-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)Oct 20, 2020

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