# Ipratropium Bromide and Albuterol Sulfate

NDC: 68788-8103
Generic name: Ipratropium Bromide and Albuterol Sulfate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20211014

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:"68788-8103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=66f32a06-c880-4b5b-837b-951e1e01e040