# Megestrol Acetate

NDC: 70954-896
Generic name: Megestrol Acetate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20240702

FDA application: ANDA077404

## Active ingredients

- MEGESTROL ACETATE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-896"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-896
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a26dcd78-ad62-4cf5-ad97-49ccb34d43ba