Product NDC: | 27808-085 |
Proprietary Name: | Dextroamphetamine |
Non Proprietary Name: | Dextroamphetamine |
Active Ingredient(s): | 5 mg/5mL & nbsp; Dextroamphetamine |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 27808-085 |
Labeler Name: | Tris Pharma Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA203644 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130531 |
Package NDC: | 27808-085-01 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (27808-085-01) |
NDC Code | 27808-085-01 |
Proprietary Name | Dextroamphetamine |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (27808-085-01) |
Product NDC | 27808-085 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dextroamphetamine |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20130531 |
Marketing Category Name | ANDA |
Labeler Name | Tris Pharma Inc |
Substance Name | DEXTROAMPHETAMINE SULFATE |
Strength Number | 5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |