# Premarin

NDC: 0046-1104
Generic name: estrogens, conjugated
Labeler / Manufacturer: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20040901

FDA application: NDA004782

## Active ingredients

- ESTROGENS, CONJUGATED: 1.25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0046-1104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0046-1104
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=258e1602-a3cf-4ccc-ca80-73dbbfb812ff
