NDC 57664-647-08
Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate 7.5 mg/1
Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate · TABLET
Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate is a tablet containing dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate at a strength of 7.5 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate
- Generic Name
- Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate
- NDC Code (Package)
57664-647-08- NDC Code (Product)
57664-647- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 7.5 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA040480
- Marketing Start
- 09/09/2003
Recall History
No Recall HistoryView Full Drug Page
Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.