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dextroamphetamine sulfate
dextroamphetamine sulfate - 58177-312-09 - (dextroamphetamine sulfate)
Drug Information of dextroamphetamine sulfate
| Product NDC: | 58177-312 |
| Proprietary Name: | dextroamphetamine sulfate |
| Non Proprietary Name: | dextroamphetamine sulfate |
| Active Ingredient(s): | 10 mg/1 & nbsp; dextroamphetamine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of dextroamphetamine sulfate
| Product NDC: | 58177-312 |
| Labeler Name: | Ethex Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040367 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091101 |
Package Information of dextroamphetamine sulfate
| Package NDC: | 58177-312-09 |
| Package Description: | 1000 TABLET in 1 BOTTLE (58177-312-09) |
NDC Information of dextroamphetamine sulfate
| NDC Code | 58177-312-09 |
| Proprietary Name | dextroamphetamine sulfate |
| Package Description | 1000 TABLET in 1 BOTTLE (58177-312-09) |
| Product NDC | 58177-312 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dextroamphetamine sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | ANDA |
| Labeler Name | Ethex Corporation |
| Substance Name | DEXTROAMPHETAMINE SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
