# Progesterone

NDC: 0143-9725
Generic name: Progesterone
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR
Marketing started: 20101028

FDA application: ANDA091033

## Active ingredients

- PROGESTERONE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9725"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9725
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=83cfc12e-75d1-4284-bcc3-beadcbd27171