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Furosemide
Furosemide - 60432-613-04 - (Furosemide)
Drug Information of Furosemide
| Product NDC: | 60432-613 |
| Proprietary Name: | Furosemide |
| Non Proprietary Name: | Furosemide |
| Active Ingredient(s): | 10 mg/mL & nbsp; Furosemide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Furosemide
| Product NDC: | 60432-613 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070655 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950101 |
Package Information of Furosemide
| Package NDC: | 60432-613-04 |
| Package Description: | 120 mL in 1 BOTTLE, WITH APPLICATOR (60432-613-04) |
NDC Information of Furosemide
| NDC Code | 60432-613-04 |
| Proprietary Name | Furosemide |
| Package Description | 120 mL in 1 BOTTLE, WITH APPLICATOR (60432-613-04) |
| Product NDC | 60432-613 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Furosemide |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19950101 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | FUROSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
