# Premarin

NDC: 0046-0749
Generic name: CONJUGATED ESTROGENS
Labeler / Manufacturer: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 19561201

FDA application: NDA010402

## Active ingredients

- ESTROGENS, CONJUGATED: 25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0046-0749"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0046-0749
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87e2da8d-432c-4ed5-67a1-dc26294b2295