# Lithium Carbonate

NDC: 72789-172
Generic name: Lithium Carbonate
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 19870128

FDA application: NDA017812

## 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:"72789-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=16ebe1f9-501d-468b-a37d-f6a46f8f32d1