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Migralex
Migralex - 49886-001-01 - (Aspirin buffered with magnesium oxide)
Drug Information of Migralex
| Product NDC: | 49886-001 |
| Proprietary Name: | Migralex |
| Non Proprietary Name: | Aspirin buffered with magnesium oxide |
| Active Ingredient(s): | 500; 75 mg/1; mg/1 & nbsp; Aspirin buffered with magnesium oxide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Migralex
| Product NDC: | 49886-001 |
| Labeler Name: | Migralex Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091115 |
Package Information of Migralex
| Package NDC: | 49886-001-01 |
| Package Description: | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (49886-001-01) |
NDC Information of Migralex
| NDC Code | 49886-001-01 |
| Proprietary Name | Migralex |
| Package Description | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (49886-001-01) |
| Product NDC | 49886-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aspirin buffered with magnesium oxide |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Migralex Inc. |
| Substance Name | ASPIRIN; MAGNESIUM OXIDE |
| Strength Number | 500; 75 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
