# EPHEDRINE SULFATE

NDC: 70069-819
Generic name: EPHEDRINE SULFATE
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20241107

FDA application: ANDA216146

## 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:"70069-819"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-819
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86b1c42c-854e-463b-ac99-4aacbbe71fd1