Details for New Drug Application (NDA): 018823
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The generic ingredient in FUROSEMIDE is furosemide. There are twenty-two drug master file entries for this compound. Fifty-eight suppliers are listed for this compound. Additional details are available on the furosemide profile page.
Summary for 018823
Tradename: | FUROSEMIDE |
Applicant: | Hikma |
Ingredient: | furosemide |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 018823
Physiological Effect | Increased Diuresis at Loop of Henle |
Medical Subject Heading (MeSH) Categories for 018823
Suppliers and Packaging for NDA: 018823
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FUROSEMIDE | furosemide | TABLET;ORAL | 018823 | NDA | Hikma Pharmaceuticals USA Inc. | 0054-4297 | 0054-4297-25 | 100 TABLET in 1 BOTTLE, PLASTIC (0054-4297-25) |
FUROSEMIDE | furosemide | TABLET;ORAL | 018823 | NDA | Hikma Pharmaceuticals USA Inc. | 0054-4297 | 0054-4297-31 | 1000 TABLET in 1 BOTTLE, PLASTIC (0054-4297-31) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Nov 10, 1983 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
Approval Date: | Nov 10, 1983 | TE: | AB | RLD: | No |
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