NDC 45802-580
Scopolamine Transdermal System 1 mg patch, extended release
On the label: Padagis Israel Pharmaceuticals Ltd.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Padagis Israel Pharmaceuticals Ltd names for other drugs.
Recalls
- May 11, 2018 · Class II · L. Perrigo Company
Defective delivery system
Lots: Lot #: a) 46397, 46457 Exp 03/19; 46621, Exp 04/19; 46894, 46904, 46905, Exp 06/19; 47133, Exp 07/19; 47153, Exp 08/19; 47154, 47213, 47214, Exp 09/19; b) 46695, Exp 04/19; 46994, 47012, Exp 07/19; 47322 10/19; c) 46822, Exp 05/19 ; 47155, 47212, Exp 09/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Scopolamine: every company that makes it
- Form
- patch, extended release, transdermal
- Strength
- 1 mg
- Approval
- ANDA ANDA078830
- On the market since
- Jun 13, 2017
- Package NDCs
45802-580-0145802-580-4645802-580-6245802-580-84- Official label
- DailyMed (National Library of Medicine), updated May 31, 2025
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