# ephedrine sulfate

NDC: 36000-336
Generic name: ephedrine sulfate
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260708

FDA application: ANDA216740

## Active ingredients

- EPHEDRINE SULFATE: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"36000-336"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=36000-336
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=552c341b-4892-4dc7-8b9f-cb6be914b0d1