# Ipratropium Bromide

NDC: 0054-0046
Generic name: Ipratropium Bromide
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20031105

FDA application: ANDA076598

## Active ingredients

- IPRATROPIUM BROMIDE: 42 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0046"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0046
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=71bdbbb9-8696-416d-bed4-7259929c0161