NDC 71335-0053 – Spironolactone
Spironolactone 25 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0053
Product details
- Brand name
- Spironolactone
- Generic name
- Spironolactone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203512
- Marketed since
- June 2, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aldosterone Antagonist
Active ingredients
- Spironolactone 25 mg/1
Uses, dosage, side effects and warnings for Spironolactone →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0053-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0053-1) | Feb 7, 2018 |
| 71335-0053-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0053-2) | Feb 22, 2019 |
| 71335-0053-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0053-3) | Feb 26, 2018 |
| 71335-0053-4 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0053-4) | Dec 27, 2021 |
| 71335-0053-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0053-5) | Oct 5, 2018 |
| 71335-0053-6 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0053-6) | Dec 27, 2021 |
| 71335-0053-7 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0053-7) | Dec 27, 2021 |
| 71335-0053-8 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0053-8) | Apr 5, 2024 |
| 71335-0053-9 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0053-9) | Apr 5, 2024 |
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