NDC 71335-0304 – Spironolactone

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

Human Prescription Drug

Product NDC71335-0304

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203512
Marketed since
June 2, 2017
Listing expires
December 31, 2027
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0304-1100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1)Feb 9, 2022
71335-0304-23 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2)Feb 9, 2022
71335-0304-330 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3)Feb 9, 2022
71335-0304-490 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4)Feb 9, 2022
71335-0304-560 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)Feb 9, 2022

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