spironolactone
- Product NDC
- 71335-1546
- 11-digit product format
- 713351546
- Labeler code
- 71335
- Product ID
- 71335-1546_12154bc1-7a03-4354-940e-ca84c13fe8ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205936
- Marketing category
- ANDA
- Marketing start
- 2018-08-15
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1546-1 | 71335154601 | 30 TABLET in 1 BOTTLE (71335-1546-1) | 30 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1546-2 | 71335154602 | 60 TABLET in 1 BOTTLE (71335-1546-2) | 60 tablet | 2020-05-20 | 0000-00-00 | No | No | Current |
| 71335-1546-3 | 71335154603 | 90 TABLET in 1 BOTTLE (71335-1546-3) | 90 tablet | 2020-04-14 | 0000-00-00 | No | No | Current |
| 71335-1546-4 | 71335154604 | 100 TABLET in 1 BOTTLE (71335-1546-4) | 100 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1546-5 | 71335154605 | 14 TABLET in 1 BOTTLE (71335-1546-5) | 14 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1546-6 | 71335154606 | 10 TABLET in 1 BOTTLE (71335-1546-6) | 10 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |