Details for New Drug Application (NDA): 211232
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NDA 211232 describes ETHACRYNIC ACID, which is a drug marketed by Adaptis, Agnitio, Alvogen, Amneal Pharms Co, Chartwell Rx, Endo Operations, Hikma, Lupin Ltd, Sciegen Pharms Inc, and Upsher Smith Labs, and is included in ten NDAs. It is available from eight suppliers. Additional details are available on the ETHACRYNIC ACID profile page.
The generic ingredient in ETHACRYNIC ACID is ethacrynic acid. There are thirteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the ethacrynic acid profile page.
The generic ingredient in ETHACRYNIC ACID is ethacrynic acid. There are thirteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the ethacrynic acid profile page.
Summary for 211232
| Tradename: | ETHACRYNIC ACID |
| Applicant: | Sciegen Pharms Inc |
| Ingredient: | ethacrynic acid |
| Patents: | 0 |
Pharmacology for NDA: 211232
| Physiological Effect | Increased Diuresis at Loop of Henle |
Medical Subject Heading (MeSH) Categories for 211232
Suppliers and Packaging for NDA: 211232
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ETHACRYNIC ACID | ethacrynic acid | TABLET;ORAL | 211232 | ANDA | ScieGen Pharmaceuticals Inc | 50228-334 | 50228-334-01 | 1000 TABLET in 1 BOTTLE (50228-334-01) |
| ETHACRYNIC ACID | ethacrynic acid | TABLET;ORAL | 211232 | ANDA | ScieGen Pharmaceuticals Inc | 50228-334 | 50228-334-10 | 100 TABLET in 1 BOTTLE (50228-334-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
| Approval Date: | Aug 27, 2019 | TE: | AB | RLD: | No | ||||
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