NDC 70518-0050

Furosemide

Furosemide

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

• Product ID: 70518-0050_800fde78-f113-f322-e053-2a91aa0a6ae8
• NDC: 70518-0050
• Product Type: Human Prescription Drug
• Proprietary Name: Furosemide
• Generic Name: Furosemide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-12-12
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077293
• Labeler Name: REMEDYREPACK 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

Packaging

NDC 70518-0050-0

30 TABLET in 1 BLISTER PACK (70518-0050-0)

• Marketing Start Date: 2016-12-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-0050-3 [70518005003]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077293
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-06-28

NDC 70518-0050-4 [70518005004]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077293
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-11-03
• Marketing End Date: 2020-04-15

NDC 70518-0050-0 [70518005000]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077293
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-12-12

NDC 70518-0050-2 [70518005002]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077293
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-02-01

NDC 70518-0050-1 [70518005001]

Furosemide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077293
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-12-30

Drug Details

Active Ingredients

Ingredient	Strength
FUROSEMIDE	20 mg/1

OpenFDA Data

• SPL SET ID: 571a52ed-5258-46d5-a0d2-9a984cf73895
• Manufacturer:
  • REMEDYREPACK 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