NDC 52584-102

Furosemide

Furosemide

Furosemide is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by General Injectables & Vaccines, Inc. The primary component is Furosemide.

• Product ID: 52584-102_bd75b5e2-d541-423a-a965-85d2197c6595
• NDC: 52584-102
• Product Type: Human Prescription Drug
• Proprietary Name: Furosemide
• Generic Name: Furosemide
• Dosage Form: Injection, Solution
• Route of Administration: INTRAMUSCULAR; INTRAVENOUS
• Marketing Start Date: 2010-08-01
• Marketing Category: NDA / NDA
• Application Number: NDA018667
• Labeler Name: General Injectables & Vaccines, Inc
• Substance Name: FUROSEMIDE
• Active Ingredient Strength: 10 mg/mL
• Pharm Classes: Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 52584-102-04

1 VIAL, SINGLE-DOSE in 1 BAG (52584-102-04) > 4 mL in 1 VIAL, SINGLE-DOSE

• Marketing Start Date: 2010-08-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52584-102-04 [52584010204]

Furosemide INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA018667
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-08-01
• Marketing End Date: 2019-07-31

NDC 52584-102-02 [52584010202]

Furosemide INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA018667
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-08-01
• Marketing End Date: 2019-07-31

NDC 52584-102-10 [52584010210]

Furosemide INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA018667
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-08-01
• Marketing End Date: 2019-10-01

Drug Details

Active Ingredients

Ingredient	Strength
FUROSEMIDE	10 mg/mL

OpenFDA Data

• SPL SET ID: 869c9eeb-baae-4189-aa5e-0b4e1ee172d2
• Manufacturer:
  • General Injectables & Vaccines, Inc
• UNII:
  • 7LXU5N7ZO5
• RxNorm Concept Unique ID - RxCUI:
  • 1719286
  • 1719290
  • 1719291

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