Furosemide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Apotheca Inc.. The primary component is Furosemide.
Product ID | 12634-416_46675cd8-ad7f-40ae-e054-00144ff8d46c |
NDC | 12634-416 |
Product Type | Human Prescription Drug |
Proprietary Name | Furosemide |
Generic Name | Furosemide |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA077293 |
Labeler Name | Apotheca Inc. |
Substance Name | FUROSEMIDE |
Active Ingredient Strength | 20 mg/1 |
Pharm Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-02-24 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Marketing Category | ANDA |
Application Number | ANDA077293 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-02-24 |
Ingredient | Strength |
---|---|
FUROSEMIDE | 20 mg/1 |
SPL SET ID: | 46675cd8-ad7e-40ae-e054-00144ff8d46c |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0054-3294 | Furosemide | Furosemide |
0054-3298 | Furosemide | Furosemide |
0054-4297 | Furosemide | Furosemide |
0054-4299 | Furosemide | Furosemide |
0054-4301 | Furosemide | Furosemide |
0054-8297 | Furosemide | Furosemide |
0054-8299 | Furosemide | Furosemide |
0054-8301 | Furosemide | Furosemide |
0378-0208 | Furosemide | furosemide |
0378-0216 | Furosemide | furosemide |
0378-0232 | Furosemide | furosemide |
0404-9861 | Furosemide | Furosemide |
0404-9862 | FUROSEMIDE | furosemide |
0404-9863 | Furosemide | Furosemide |
0404-9864 | FUROSEMIDE | furosemide |
0409-1639 | Furosemide | FUROSEMIDE |
0409-6102 | FUROSEMIDE | FUROSEMIDE |
68071-1708 | Furosemide | Furosemide |
68071-1809 | Furosemide | Furosemide |
68071-3273 | Furosemide | Furosemide |
68071-3144 | Furosemide | Furosemide |
68071-3194 | Furosemide | Furosemide |
68071-3148 | Furosemide | Furosemide |
68071-4015 | Furosemide | Furosemide |
68071-4022 | Furosemide | Furosemide |
68071-4349 | Furosemide | Furosemide |
68071-4534 | Furosemide | Furosemide |
0409-9631 | Furosemide | Furosemide |
68071-4445 | Furosemide | Furosemide |
68071-4522 | Furosemide | Furosemide |
68094-867 | Furosemide | Furosemide |
68094-756 | Furosemide | Furosemide |
68788-1966 | Furosemide | Furosemide |
68788-6397 | Furosemide | Furosemide |
68788-6784 | Furosemide | Furosemide |
68788-7265 | Furosemide | Furosemide |
68788-6948 | Furosemide | Furosemide |
68788-9226 | Furosemide | Furosemide |
68788-7354 | Furosemide | Furosemide |
68788-9778 | Furosemide | Furosemide |
69315-116 | Furosemide | Furosemide |
69315-118 | Furosemide | Furosemide |
69315-117 | Furosemide | Furosemide |
69677-204 | Furosemide | Furosemide |
70121-1164 | Furosemide | Furosemide |
70121-1076 | Furosemide | Furosemide |
70121-1163 | Furosemide | Furosemide |
70518-0092 | Furosemide | Furosemide |
70518-0584 | Furosemide | Furosemide |
70518-0120 | Furosemide | Furosemide |