# Scopolamine

NDC: 42858-150
Generic name: Scopolamine
Labeler / Manufacturer: Rhodes Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20241101

FDA application: ANDA215329

## Active ingredients

- SCOPOLAMINE: 1 mg/3d

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42858-150"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42858-150
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba5a1237-4d23-441a-808e-96b97045fbe2