# AfterPlan

NDC: 62756-723
Generic name: levonorgestrel
Labeler / Manufacturer: SUN PHARMACEUTICAL INDUSTRIES, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170512

FDA application: ANDA202635

## Active ingredients

- LEVONORGESTREL: 1.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62756-723"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62756-723
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c30c7bc2-04fa-4590-96f5-5bcf4bba3f1a