# lamivudine

NDC: 68999-706
Generic name: lamivudine oral
Labeler / Manufacturer: Chartwell Govermental & Specialty RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20141031

FDA application: ANDA203564

## Active ingredients

- LAMIVUDINE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68999-706"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-706
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b23aea53-324b-4ff2-8736-639e4045e388