NDC 72162-1626 – Spironolactone
Spironolactone 50 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-1626
Product details
- Brand name
- Spironolactone
- Generic name
- Spironolactone
- Labeler
- Bryant Ranch Prepack
- 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 50 mg/1
Uses, dosage, side effects and warnings for Spironolactone →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1626-1 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-1626-1) | Mar 27, 2026 |
| 72162-1626-3 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1626-3) | Mar 27, 2026 |
| 72162-1626-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-1626-5) | Mar 27, 2026 |
| 72162-1626-6 | 60 TABLET, FILM COATED in 1 BOTTLE (72162-1626-6) | Mar 27, 2026 |
| 72162-1626-9 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-1626-9) | Mar 27, 2026 |
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