NDC 0378-2146 – Spironolactone

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

Human Prescription Drug

Product NDC0378-2146

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040424
Marketed since
February 3, 1981
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
0378-2146-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2146-01)Feb 3, 1981
0378-2146-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2146-05)Feb 3, 1981

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