Furosemide

Product NDC: 58517-400
11-digit product format: 585170400
Labeler code: 58517
Product ID: 58517-400_fa87df49-449e-4062-be6e-6b85da718a1b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Furosemide
Dosage form: TABLET
Route: ORAL
Labeler: New Horizon Rx Group, LLC
Application: ANDA078010
Marketing category: ANDA
Marketing start: 2013-08-25
Marketing end: 0000-00-00
Substance: FUROSEMIDE
Active strength: 40 mg/1
Pharmacologic classes: Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

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

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58517-400-30	2019-11-27	C162847	48780-1	9855e2a2-3b67-60a7-e053-dbdaa90a05bd	Furosemide Tablets, USP Rx only

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58517-400-30	Furosemide	30 in 1 BOTTLE	TABLET	30		2

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
58517-400-30	EA - Each	58517-400	ebbbe8c4-7f59-463a-9979-ffcccdcff289	1	2013-11-04

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FUROSEMIDE	ACTIVE INGREDIENT	7LXU5N7ZO5	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
FUROSEMIDE	ACTIVE MOIETY	7LXU5N7ZO5	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58517-400	FUROSEMIDE TABLET [NEW HORIZON RX GROUP, LLC]	2	Legacy NDC, 1 package rows	20131231_4b635500-474a-4944-a66a-b305443344ae.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	4b635500-474a-4944-a66a-b305443344ae	2
313988	furosemide 40 MG Oral Tablet	SCD	4b635500-474a-4944-a66a-b305443344ae	2

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
58517-400-30	58517040030	30 in 1 BOTTLE	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Furosemide Tablets, USP Rx only	New Horizon Rx Group, LLC \| Ipca Laboratories Limited	2013-12-31	HUMAN PRESCRIPTION DRUG LABEL	2