NDC 68788-7265

Furosemide

Furosemide

Furosemide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Furosemide.

• Product ID: 68788-7265_07d79cb6-cd35-4f3f-ab2e-63038fcc418b
• NDC: 68788-7265
• Product Type: Human Prescription Drug
• Proprietary Name: Furosemide
• Generic Name: Furosemide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2018-09-24
• Marketing Category: ANDA / ANDA
• Application Number: ANDA076796
• Labeler Name: Preferred Pharmaceuticals 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: 2021-12-31

Packaging

NDC 68788-7265-1

100 TABLET in 1 BOTTLE, PLASTIC (68788-7265-1)

• Marketing Start Date: 2018-09-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-7265-6 [68788726506]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA076796
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-09-24

NDC 68788-7265-1 [68788726501]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA076796
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-09-24

NDC 68788-7265-3 [68788726503]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA076796
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-09-24

NDC 68788-7265-9 [68788726509]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA076796
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-09-24

Drug Details

Active Ingredients

Ingredient	Strength
FUROSEMIDE	20 mg/1

OpenFDA Data

• SPL SET ID: 9ea83ce1-fee0-484c-909f-83671d3a4f33
• Manufacturer:
  • Preferred Pharmaceuticals Inc.
• UNII:
  • 7LXU5N7ZO5
• RxNorm Concept Unique ID - RxCUI:
  • 310429

Pharmacological Class

• Increased Diuresis at Loop of Henle [PE]
• Loop Diuretic [EPC]

NDC Crossover Matching brand name "Furosemide" or generic name "Furosemide"

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