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ProCentra
ProCentra - 13551-701-05 - (dextroamphetamine sulfate)
Drug Information of ProCentra
| Product NDC: | 13551-701 |
| Proprietary Name: | ProCentra |
| Non Proprietary Name: | dextroamphetamine sulfate |
| Active Ingredient(s): | 5 mg/5mL & nbsp; dextroamphetamine sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ProCentra
| Product NDC: | 13551-701 |
| Labeler Name: | FSC Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040776 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100801 |
Package Information of ProCentra
| Package NDC: | 13551-701-05 |
| Package Description: | 473 mL in 1 BOTTLE (13551-701-05) |
NDC Information of ProCentra
| NDC Code | 13551-701-05 |
| Proprietary Name | ProCentra |
| Package Description | 473 mL in 1 BOTTLE (13551-701-05) |
| Product NDC | 13551-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dextroamphetamine sulfate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100801 |
| Marketing Category Name | ANDA |
| Labeler Name | FSC Laboratories, Inc |
| Substance Name | DEXTROAMPHETAMINE SULFATE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
