# PROGESTERONE

NDC: 0591-3128
Generic name: PROGESTERONE
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 19780511

FDA application: NDA017362

## Active ingredients

- PROGESTERONE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0591-3128"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0591-3128
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a09a3b76-36f1-4d20-930e-7e3da97e7ebd