NDC 68382-662 – Spironolactone

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

Human Prescription Drug

Product NDC68382-662

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205936
Marketed since
August 15, 2018
Listing expires
December 31, 2026
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (6)

Package NDCDescriptionSince
68382-662-01100 TABLET, FILM COATED in 1 BOTTLE (68382-662-01)Aug 15, 2018
68382-662-05500 TABLET, FILM COATED in 1 BOTTLE (68382-662-05)Aug 15, 2018
68382-662-0630 TABLET, FILM COATED in 1 BOTTLE (68382-662-06)Aug 15, 2018
68382-662-101000 TABLET, FILM COATED in 1 BOTTLE (68382-662-10)Aug 15, 2018
68382-662-1690 TABLET, FILM COATED in 1 BOTTLE (68382-662-16)Aug 15, 2018
68382-662-3010 BLISTER PACK in 1 CARTON (68382-662-30) / 10 TABLET, FILM COATED in 1 BLISTER PACKAug 15, 2018

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