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Spironolactone
Spironolactone - 51079-103-19 - (spironolactone)
Drug Information of Spironolactone
| Product NDC: | 51079-103 |
| Proprietary Name: | Spironolactone |
| Non Proprietary Name: | spironolactone |
| Active Ingredient(s): | 25 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: | 51079-103 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040424 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110204 |
Package Information of Spironolactone
| Package NDC: | 51079-103-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-103-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-103-17) |
NDC Information of Spironolactone
| NDC Code | 51079-103-19 |
| Proprietary Name | Spironolactone |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-103-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-103-17) |
| Product NDC | 51079-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | spironolactone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110204 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | SPIRONOLACTONE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA] |
