# Nortrel 7/7/7 (28 Day Regimen)

NDC: 0555-9012
Generic name: Norethindrone and Ethinyl Estradiol
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20030102

FDA application: ANDA075478

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0555-9012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0555-9012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=992dcc56-90ab-4691-8114-16d47a8b9982