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Diurex
Diurex - 52389-306-22 - (Caffeine, magnesium salicylate)
Drug Information of Diurex
| Product NDC: | 52389-306 |
| Proprietary Name: | Diurex |
| Non Proprietary Name: | Caffeine, magnesium salicylate |
| Active Ingredient(s): | 50; 162.5 mg/1; mg/1 & nbsp; Caffeine, magnesium salicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diurex
| Product NDC: | 52389-306 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050515 |
Package Information of Diurex
| Package NDC: | 52389-306-22 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (52389-306-22) > 11 TABLET, COATED in 1 BLISTER PACK (52389-306-02) |
NDC Information of Diurex
| NDC Code | 52389-306-22 |
| Proprietary Name | Diurex |
| Package Description | 2 BLISTER PACK in 1 CARTON (52389-306-22) > 11 TABLET, COATED in 1 BLISTER PACK (52389-306-02) |
| Product NDC | 52389-306 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Caffeine, magnesium salicylate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050515 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | CAFFEINE; MAGNESIUM SALICYLATE |
| Strength Number | 50; 162.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
