Home
>
National Drug Code (NDC)
>
spironolactone
spironolactone - 43063-277-30 - (spironolactone)
Drug Information of spironolactone
| Product NDC: | 43063-277 |
| Proprietary Name: | spironolactone |
| Non Proprietary Name: | spironolactone |
| Active Ingredient(s): | 50 mg/1 & nbsp; spironolactone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of spironolactone
| Product NDC: | 43063-277 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012151 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19600121 |
Package Information of spironolactone
| Package NDC: | 43063-277-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-277-30) |
NDC Information of spironolactone
| NDC Code | 43063-277-30 |
| Proprietary Name | spironolactone |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-277-30) |
| Product NDC | 43063-277 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | spironolactone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19600121 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | SPIRONOLACTONE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA] |
