# Ipratropium Bromide and Albuterol Sulfate

NDC: 47335-756
Generic name: Ipratropium Bromide and Albuterol Sulfate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20211115

FDA application: ANDA207875

## Active ingredients

- ALBUTEROL SULFATE: 2.5 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:"47335-756"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-756
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=38f9a201-3954-4370-8e71-7ec2df88a1ff