NDC 43063-832 – Spironolactone

Spironolactone 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC43063-832

Product details

Brand name
Spironolactone
Generic name
spironolactone
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
43063-832-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-01)Jan 31, 2018
43063-832-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-30)Jan 31, 2018
43063-832-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-60)Jun 12, 2018
43063-832-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-90)Jan 31, 2018

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