NDC 71335-2366 – Spironolactone
Spironolactone 25 mg/1 · Tablet · Oral
Product NDC71335-2366
Product details
- Brand name
- Spironolactone
- Generic name
- Spironolactone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA089424
- Marketed since
- July 23, 1986
- 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 |
|---|---|---|
| 71335-2366-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2366-1) | Apr 30, 2024 |
| 71335-2366-2 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2366-2) | Apr 30, 2024 |
| 71335-2366-3 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2366-3) | Apr 30, 2024 |
| 71335-2366-4 | 14 TABLET in 1 BOTTLE, PLASTIC (71335-2366-4) | Apr 30, 2024 |
| 71335-2366-5 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2366-5) | Apr 30, 2024 |
| 71335-2366-6 | 7 TABLET in 1 BOTTLE, PLASTIC (71335-2366-6) | Apr 30, 2024 |
| 71335-2366-7 | 10 TABLET in 1 BOTTLE, PLASTIC (71335-2366-7) | Apr 30, 2024 |
| 71335-2366-8 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-2366-8) | Apr 30, 2024 |
| 71335-2366-9 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-2366-9) | Apr 30, 2024 |
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