NDC 68382-660 – spironolactone
Spironolactone 25 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-660
Product details
- Brand name
- spironolactone
- Generic name
- spironolactone
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- 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 |
|---|---|---|
| 68382-660-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-660-01) | Aug 15, 2018 |
| 68382-660-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-660-05) | Aug 15, 2018 |
| 68382-660-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-660-06) | Aug 15, 2018 |
| 68382-660-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-660-10) | Aug 15, 2018 |
| 68382-660-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-660-16) | Aug 15, 2018 |
| 68382-660-30 | 10 BLISTER PACK in 1 CARTON (68382-660-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Aug 15, 2018 |
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