# Levocarnitine

NDC: 16571-762
Generic name: Levocarnitine
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201201

FDA application: ANDA076858

## Active ingredients

- LEVOCARNITINE: 330 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-762"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-762
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f749812-8f02-4eeb-91d9-5dd6fc9fa159