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NDC 23155-0763-05 Lithium carbonate 300 mg/1 Details

Lithium carbonate 300 mg/1

Lithium carbonate is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is LITHIUM CARBONATE.

MedlinePlus Drug Summary

Lithium is used to treat and prevent episodes of mania (frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). Lithium is in a class of medications called antimanic agents. It works by decreasing abnormal activity in the brain.

Related Packages: 23155-0763-05
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Lithium

Product Information

NDC	23155-0763
Product ID	23155-763_9050ff15-5fa6-4c8b-b312-aedf4fd6175b
Associated GPIs	59500010100405
GCN Sequence Number	004004
GCN Sequence Number Description	lithium carbonate TABLET ER 300 MG ORAL
HIC3	H2M
HIC3 Description	BIPOLAR DISORDER DRUGS
GCN	15731
HICL Sequence Number	001669
HICL Sequence Number Description	LITHIUM CARBONATE
Brand/Generic	Generic
Proprietary Name	Lithium carbonate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Lithium carbonate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	300
Active Ingredient Units	mg/1
Substance Name	LITHIUM CARBONATE
Labeler Name	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Pharmaceutical Class	Mood Stabilizer [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA205532
Listing Certified Through	2024-12-31

Package

NDC 23155-0763-05 (23155076305)

Pricing Information	N/A
NDC Package Code	23155-763-05
Billing NDC	23155076305
Package	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)
Marketing Start Date	2020-10-20
NDC Exclude Flag	N