Home
>
National Drug Code (NDC)
>
Diurex
Diurex - 52389-613-42 - (Caffeine)
Drug Information of Diurex
| Product NDC: | 52389-613 |
| Proprietary Name: | Diurex |
| Non Proprietary Name: | Caffeine |
| Active Ingredient(s): | 200 mg/1 & nbsp; Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diurex
| Product NDC: | 52389-613 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part357 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090415 |
Package Information of Diurex
| Package NDC: | 52389-613-42 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (52389-613-42) > 21 TABLET, FILM COATED in 1 BLISTER PACK (52389-613-01) |
NDC Information of Diurex
| NDC Code | 52389-613-42 |
| Proprietary Name | Diurex |
| Package Description | 2 BLISTER PACK in 1 CARTON (52389-613-42) > 21 TABLET, FILM COATED in 1 BLISTER PACK (52389-613-01) |
| Product NDC | 52389-613 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Caffeine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090415 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | CAFFEINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
