NDC 53489-329 – Spironolactone
Spironolactone 100 mg/1 · Tablet, Film Coated · Oral
Product NDC53489-329
Product details
- Brand name
- Spironolactone
- Generic name
- Spironolactone
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA089424
- Marketed since
- July 23, 1986
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aldosterone Antagonist
Active ingredients
- Spironolactone 100 mg/1
Uses, dosage, side effects and warnings for Spironolactone →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 53489-329-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-01) | Jul 23, 1986 |
| 53489-329-02 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-02) | Jul 23, 1986 |
| 53489-329-03 | 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-03) | Jul 23, 1986 |
| 53489-329-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-05) | Jul 23, 1986 |
| 53489-329-10 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-10) | Jul 23, 1986 |
Recalls mentioning this NDC
- D-0574-2025 Aug 13, 2025 · Class II
Presence of foreign substance: identified as aluminum.
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