Furosemide

Product NDC: 50090-3488
11-digit product format: 500903488
Labeler code: 50090
Product ID: 50090-3488_be05fc5d-5269-4c38-b749-483b6f6b8f32
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: furosemide
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA076796
Marketing category: ANDA
Marketing start: 2004-03-26
Marketing end: 0000-00-00
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: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50090-3488-0	2023-02-07	C162847	48780-1	f386c64a-1548-0266-e053-dadaa90a7c1a	b8bb2a76-8ed3-488a-9152-c7da076f0d65
50090-3488-0	2023-01-30	C162847	48780-1	f386c64a-1548-0266-e053-dadaa90a7c1a	b8bb2a76-8ed3-488a-9152-c7da076f0d65

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

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50090-3488-0	50090348800	100 TABLET in 1 BOTTLE, PLASTIC (50090-3488-0)	100 tablet	2018-06-18	0000-00-00	No	No	Current