# Scopolamine

NDC: 70710-1846
Generic name: Scopolamine
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20240905

FDA application: ANDA217893

## 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:"70710-1846"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1846
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62d8332e-b8d2-4d13-8071-978d57e51928