# Lanthanum carbonate

NDC: 0093-5940
Generic name: Lanthanum carbonate
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20220525

FDA application: ANDA090977

## Active ingredients

- LANTHANUM CARBONATE: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-5940"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-5940
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4b88992-ecb0-455b-b68c-5c4e6d3cf521