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Stagesic
Stagesic - 58407-091-01 - (hydrocodone bitartrate and acetaminophen)
Drug Information of Stagesic
| Product NDC: | 58407-091 |
| Proprietary Name: | Stagesic |
| Non Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 500; 5 mg/1; mg/1 & nbsp; hydrocodone bitartrate and acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stagesic
| Product NDC: | 58407-091 |
| Labeler Name: | Magna Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089008 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990607 |
Package Information of Stagesic
| Package NDC: | 58407-091-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (58407-091-01) |
NDC Information of Stagesic
| NDC Code | 58407-091-01 |
| Proprietary Name | Stagesic |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (58407-091-01) |
| Product NDC | 58407-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19990607 |
| Marketing Category Name | ANDA |
| Labeler Name | Magna Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 500; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
