FUROSEMIDE

Product NDC: 61919-442
11-digit product format: 619190442
Labeler code: 61919
Product ID: 61919-442_a8ea7cbf-8e51-cc9b-e053-2a95a90aa751
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: FUROSEMIDE
Dosage form: TABLET
Route: ORAL
Labeler: DIRECT RX
Application: ANDA076796
Marketing category: ANDA
Marketing start: 2014-01-01
Marketing end: 0000-00-00
Substance: FUROSEMIDE
Active strength: 20 mg/1
Pharmacologic classes: Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
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
61919-442-30	2025-01-31	C162847	48780-1	1030e365-2e53-111a-e063-dadaa90a10e2	FUROSEMIDE
61919-442-30	2024-01-30	C162847	48780-1	1030e365-2e53-111a-e063-dadaa90a10e2	FUROSEMIDE

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61919-442-30	FUROSEMIDE	30 in 1 BOTTLE	TABLET	30		6

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
61919-442-30	EA - Each	61919-442	438df933-2318-4818-b0a5-d918d7f3d650	1	2014-11-05

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FUROSEMIDE	ACTIVE INGREDIENT	7LXU5N7ZO5	FUROSEMIDE TABLET [DIRECT RX]	1
FUROSEMIDE	ACTIVE MOIETY	7LXU5N7ZO5	FUROSEMIDE TABLET [DIRECT RX]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	FUROSEMIDE TABLET [DIRECT RX]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	FUROSEMIDE TABLET [DIRECT RX]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	FUROSEMIDE TABLET [DIRECT RX]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	FUROSEMIDE TABLET [DIRECT RX]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61919-442	FUROSEMIDE TABLET [DIRECT RX]	5	Legacy NDC, 1 package rows	20200626_9ec7808e-9201-4b8c-9790-d329320dc6c4.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
310429	furosemide 20 MG Oral Tablet	PSN	9ec7808e-9201-4b8c-9790-d329320dc6c4	6
310429	furosemide 20 MG Oral Tablet	SCD	9ec7808e-9201-4b8c-9790-d329320dc6c4	6

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61919-442-30	61919044230	30 TABLET in 1 BOTTLE (61919-442-30)	30 tablet	2015-01-01	0000-00-00	No	No	Current