# My After Plan

NDC: 51660-098
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: 20260901

FDA application: ANDA207660

## 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:"51660-098"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-098