Details for New Drug Application (NDA): 078010
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The generic ingredient in FUROSEMIDE is furosemide. There are twenty-two drug master file entries for this compound. Fifty-five suppliers are listed for this compound. Additional details are available on the furosemide profile page.
Summary for 078010
Tradename: | FUROSEMIDE |
Applicant: | Ipca Labs Ltd |
Ingredient: | furosemide |
Patents: | 0 |
Pharmacology for NDA: 078010
Physiological Effect | Increased Diuresis at Loop of Henle |
Medical Subject Heading (MeSH) Categories for 078010
Suppliers and Packaging for NDA: 078010
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
FUROSEMIDE | furosemide | TABLET;ORAL | 078010 | ANDA | Proficient Rx LP | 63187-097 | 63187-097-30 | 30 TABLET in 1 BLISTER PACK (63187-097-30) |
FUROSEMIDE | furosemide | TABLET;ORAL | 078010 | ANDA | Proficient Rx LP | 63187-437 | 63187-437-90 | 90 TABLET in 1 BLISTER PACK (63187-437-90) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Sep 18, 2006 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 40MG | ||||
Approval Date: | Sep 18, 2006 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 80MG | ||||
Approval Date: | Sep 18, 2006 | TE: | AB | RLD: | No |
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