NDC 0228-3062 – Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
Dextroamphetamine Saccharate 1.25 mg/1; Amphetamine Aspartate Monohydrate 1.25 mg/1; Dextroamphetamine Sulfate 1.25 mg/1; Amphetamine Sulfate 1.25 mg/1 · Capsule, Extended Release · Oral
Product NDC0228-3062
Product details
- Brand name
- Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
- Generic name
- Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077302
- Marketed since
- June 22, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Central Nervous System Stimulant; Central Nervous System Stimulant; Central Nervous System Stimulant; Central Nervous System Stimulant
Active ingredients
- Dextroamphetamine Saccharate 1.25 mg/1
- Amphetamine Aspartate Monohydrate 1.25 mg/1
- Dextroamphetamine Sulfate 1.25 mg/1
- Amphetamine Sulfate 1.25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0228-3062-11 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-3062-11) | Jun 22, 2012 |
Recalls mentioning this NDC
- D-190-2013 Mar 13, 2013 · Class III
Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met.
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