NDC 0185-2099
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate 4 ingredients tablet
On the label: Sandoz Inc..
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 Sandoz Inc. names for other drugs.
Product details
- Generic drug
- Amphetamine and Dextroamphetamine: every company that makes it
- Form
- tablet, oral
- Strength
- 4 ingredients
- Approval
- ANDA ANDA040439
- On the market since
- Jun 14, 2002
- Package NDCs
0185-2099-01- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2024
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