NDC 51655-344 – Spironolactone

Spironolactone 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-344

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203512
Marketed since
May 27, 2020
Listing expires
December 31, 2027
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (2)

Package NDCDescriptionSince
51655-344-2690 TABLET, FILM COATED in 1 BOTTLE (51655-344-26)May 27, 2020
51655-344-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-344-52)Aug 24, 2020

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