# Progesterone

NDC: 71205-669
Generic name: Progesterone
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210108

FDA application: ANDA205229

## Active ingredients

- PROGESTERONE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-669"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-669
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80a63b2b-96be-423d-abbd-13acc802f6da
