Furosemide

Product NDC: 51079-527
11-digit product format: 510790527
Labeler code: 51079
Product ID: 51079-527_d347d4b5-8000-f23e-e053-2a95a90a9ad0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: furosemide
Dosage form: TABLET
Route: ORAL
Labeler: Mylan Institutional Inc.
Application: ANDA070082
Marketing category: ANDA
Marketing start: 1997-02-06
Marketing end: 2030-01-31
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: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51079-527-01	EA - Each	51079-527	4c93fd5b-8eea-493a-8b1c-43fe065f7d36	1	2012-07-24
51079-527-17	EA - Each	51079-527	39e6cc37-a23a-417d-9e32-8ac865d63c99	1	2012-07-24
51079-527-19	EA - Each	51079-527	0fe5962e-0207-49f9-8a68-40b21118a52f	1	2012-07-24
51079-527-20	EA - Each	51079-527	26ff5673-64cd-4ef1-95a6-3029fef78107	1	2012-07-24

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
51079-527-20	51079052720	100 BLISTER PACK in 1 CARTON (51079-527-20) > 1 TABLET in 1 BLISTER PACK (51079-527-01)	100 blister pack	1997-02-06	0000-00-00	No	No	Current