# Lithium Carbonate

NDC: 70518-2312
Generic name: Lithium Carbonate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190913

FDA application: ANDA079139

## Active ingredients

- LITHIUM CARBONATE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2312"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2312
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=803eab29-0d0a-4df0-b504-bcd85ec01ead