# Terbutaline Sulfate

NDC: 63323-665
Generic name: TERBUTALINE SULFATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20110310

FDA application: ANDA076887

## Active ingredients

- TERBUTALINE SULFATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-665"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-665
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cec31032-f366-4524-9e01-63146e473b2b