# Lithium Carbonate

NDC: 50090-6052
Generic name: lithium carbonate
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20120702

FDA application: ANDA202288

## Active ingredients

- LITHIUM CARBONATE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-6052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-6052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=baf59ee7-1c98-4f77-96c5-7b50b7acb8f4