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Relagesic
Relagesic - 11584-0476-1 - (Acetaminophen and Phenyltoloxamine Citrate)
Drug Information of Relagesic
| Product NDC: | 11584-0476 |
| Proprietary Name: | Relagesic |
| Non Proprietary Name: | Acetaminophen and Phenyltoloxamine Citrate |
| Active Ingredient(s): | 650; 50 mg/1; mg/1 & nbsp; Acetaminophen and Phenyltoloxamine Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Relagesic
| Product NDC: | 11584-0476 |
| Labeler Name: | International Ethical Labs, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19950916 |
Package Information of Relagesic
| Package NDC: | 11584-0476-1 |
| Package Description: | 100 TABLET in 1 BOTTLE, DISPENSING (11584-0476-1) |
NDC Information of Relagesic
| NDC Code | 11584-0476-1 |
| Proprietary Name | Relagesic |
| Package Description | 100 TABLET in 1 BOTTLE, DISPENSING (11584-0476-1) |
| Product NDC | 11584-0476 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetaminophen and Phenyltoloxamine Citrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19950916 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | International Ethical Labs, inc. |
| Substance Name | ACETAMINOPHEN; PHENYLTOLOXAMINE CITRATE |
| Strength Number | 650; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
