# Morning After

NDC: 69953-515
Generic name: Levonorgestrel
Labeler / Manufacturer: Rapha Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180322

FDA application: ANDA206867

## Active ingredients

- LEVONORGESTREL: 1.5 mg/1.5mg

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69953-515"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69953-515
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=677aa953-3c30-4ce5-e053-2991aa0ab2b2