NDC 68382-660 – spironolactone

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

Human Prescription Drug

Product NDC68382-660

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
68382-660-01100 TABLET, FILM COATED in 1 BOTTLE (68382-660-01)Aug 15, 2018
68382-660-05500 TABLET, FILM COATED in 1 BOTTLE (68382-660-05)Aug 15, 2018
68382-660-0630 TABLET, FILM COATED in 1 BOTTLE (68382-660-06)Aug 15, 2018
68382-660-101000 TABLET, FILM COATED in 1 BOTTLE (68382-660-10)Aug 15, 2018
68382-660-1690 TABLET, FILM COATED in 1 BOTTLE (68382-660-16)Aug 15, 2018
68382-660-3010 BLISTER PACK in 1 CARTON (68382-660-30) / 10 TABLET, FILM COATED in 1 BLISTER PACKAug 15, 2018

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