# Ipratropium Bromide and Albuterol Sulfate

NDC: 0487-0201
Generic name: Ipratropium Bromide and Albuterol Sulfate
Labeler / Manufacturer: Nephron Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20071231

FDA application: ANDA076749

## Active ingredients

- ALBUTEROL SULFATE: 3 mg/3mL
- IPRATROPIUM BROMIDE: .5 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0487-0201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0487-0201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae35ec1f-526a-49bf-8262-c50e40190d1f