NDC 70771-1027 – spironolactone
Spironolactone 25 mg/1 · Tablet, Film Coated · Oral
Product NDC70771-1027
Product details
- Brand name
- spironolactone
- Generic name
- spironolactone
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205936
- Marketed since
- August 15, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aldosterone Antagonist
Active ingredients
- Spironolactone 25 mg/1
Uses, dosage, side effects and warnings for Spironolactone →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1027-0 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1027-0) | Aug 15, 2018 |
| 70771-1027-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1027-1) | Aug 15, 2018 |
| 70771-1027-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1027-3) | Aug 15, 2018 |
| 70771-1027-4 | 10 BLISTER PACK in 1 CARTON (70771-1027-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Aug 15, 2018 |
| 70771-1027-5 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1027-5) | Aug 15, 2018 |
| 70771-1027-9 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1027-9) | Aug 15, 2018 |
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