# Levonorgestrel

NDC: 51660-999
Generic name: Levonorgestrel
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171101

FDA application: ANDA202635

## Active ingredients

- LEVONORGESTREL: 1.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51660-999"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-999
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3f2a41a-a9af-4d63-81d8-33181d12af40