spironolactone
- Product NDC
- 70518-4468
- 11-digit product format
- 705184468
- Labeler code
- 70518
- Product ID
- 70518-4468_471a230b-39a8-89e1-e063-6394a90a1184
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205936
- Marketing category
- ANDA
- Marketing start
- 2025-09-07
- Substance
- SPIRONOLACTONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 27O7W4T232 | SPIRONOLACTONE | 52-01-7 | SPIRONOLACTONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4468-0 | 70518446800 | 100 POUCH in 1 BOX (70518-4468-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4468-1) | 100 pouch | 2025-09-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| spironolactone | REMEDYREPACK INC. | 2025-12-29 | HUMAN PRESCRIPTION DRUG LABEL | 3 |