# METHSCOPOLAMINE BROMIDE

NDC: 72319-030
Generic name: methscopolamine bromide
Labeler / Manufacturer: i3 Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241218

FDA application: ANDA216786

## Active ingredients

- METHSCOPOLAMINE BROMIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72319-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72319-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14c0c030-e96d-4a5e-95ff-02dd78a46be3