SPIRONOLACTONE
- Product NDC
- 71205-830
- 11-digit product format
- 712050830
- Labeler code
- 71205
- Product ID
- 71205-830_416ce231-fc8d-4ba0-a1ce-d5e054cf025e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SPIRONOLACTONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA089424
- Marketing category
- ANDA
- Marketing start
- 1986-07-23
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-830-30 | 71205083030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-30) | 2023-08-18 | No | No | Historical |
| 71205-830-60 | 71205083060 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-60) | 2023-08-18 | No | No | Historical |
| 71205-830-90 | 71205083090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-830-90) | 2023-08-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| SPIRONOLACTONE | Proficient Rx LP | 2023-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |