Furosemide

Product NDC: 69315-118
11-digit product format: 693150118
Labeler code: 69315
Product ID: 69315-118_445bfa17-a52c-4492-9dbc-94218b30c1db
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Furosemide
Dosage form: TABLET
Route: ORAL
Labeler: Leading Pharma, LLC
Application: ANDA077293
Marketing category: ANDA
Marketing start: 2006-02-01
Substance: FUROSEMIDE
Active strength: 80 mg/1
Pharmacologic classes: Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Ingredient, Strength table
Ingredient	Strength
FUROSEMIDE	80 mg/1

Field, Values table
Field	Values
Unii	7LXU5N7ZO5
Rxcui	197732, 310429, 313988

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d80d3aff-3a63-4d7b-a2be-fd9388b04330	Product name	9	20250806
9061e89f-9c86-4196-b34b-886fc1673cc4	Product name	1	20140821

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69315-118-01	Furosemide	100 in 1 BOTTLE	TABLET	100		10
69315-118-05	Furosemide	500 in 1 BOTTLE	TABLET	500		10

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69315-118-01	EA - Each	69315-118	341b149a-7f04-4a89-afd5-5d34a015957a	1	2016-05-16
69315-118-05	EA - Each	69315-118	f899a81e-1ef0-4479-bf1a-445420eb4efc	1	2016-05-16

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69315-118	FUROSEMIDE (FUROSEMIDE) TABLET [LEADING PHARMA, LLC]	10	Current NDC, Legacy NDC, 2 package rows	20221117_b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7LXU5N7ZO5	FUROSEMIDE	54-31-9	FUROSEMIDE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313988	furosemide 40 MG Oral Tablet	PSN	83662449-f2b1-48a3-9021-13037e64e6ea	19
197732	furosemide 80 MG Oral Tablet	PSN	83662449-f2b1-48a3-9021-13037e64e6ea	19
313988	furosemide 40 MG Oral Tablet	SCD	83662449-f2b1-48a3-9021-13037e64e6ea	19
197732	furosemide 80 MG Oral Tablet	SCD	83662449-f2b1-48a3-9021-13037e64e6ea	19
310429	furosemide 20 MG Oral Tablet	PSN	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
313988	furosemide 40 MG Oral Tablet	PSN	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
197732	furosemide 80 MG Oral Tablet	PSN	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
310429	furosemide 20 MG Oral Tablet	SCD	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
313988	furosemide 40 MG Oral Tablet	SCD	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
197732	furosemide 80 MG Oral Tablet	SCD	b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe	10
197732	furosemide 80 MG Oral Tablet	PSN	33ec71e2-8fbd-0703-e063-6294a90a62e1	1
197732	furosemide 80 MG Oral Tablet	SCD	33ec71e2-8fbd-0703-e063-6294a90a62e1	1

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69315-118-01	69315011801	100 TABLET in 1 BOTTLE (69315-118-01)	100 tablet	2016-05-15	0000-00-00	No	No	Current
69315-118-05	69315011805	500 TABLET in 1 BOTTLE (69315-118-05)	500 tablet	2016-05-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
FUROSEMIDE TABLETS, USP 20 mg, 40 mg and 80 mg	Coupler LLC	2025-04-29	HUMAN PRESCRIPTION DRUG LABEL	1
FUROSEMIDE TABLETS, USP 20 mg, 40 mg and 80 mg	A-S Medication Solutions	2024-04-23	HUMAN PRESCRIPTION DRUG LABEL	19
FUROSEMIDE TABLETS, USP 20 mg, 40 mg and 80 mg	Leading Pharma, LLC	2022-11-11	HUMAN PRESCRIPTION DRUG LABEL	10