# Prempro

NDC: 0046-1107
Generic name: conjugated estrogens and medroxyprogesterone acetate
Labeler / Manufacturer: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, SUGAR COATED
Routes: ORAL
Marketing started: 20090921

FDA application: NDA020527

## Active ingredients

- ESTROGENS, CONJUGATED: .625 mg/1
- MEDROXYPROGESTERONE ACETATE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0046-1107"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0046-1107
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd0c0836-5d23-2183-da81-9dc7f4287052