# Progesterone

NDC: 63323-261
Generic name: PROGESTERONE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20010719

FDA application: ANDA075906

## 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:"63323-261"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-261
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a479b395-1e1a-4d2a-8feb-68a15c47225f