SPIRONOLACTONE
- Product NDC
- 63629-1063
- 11-digit product format
- 636291063
- Labeler code
- 63629
- Product ID
- 63629-1063_1605803d-7043-499f-a6ee-9befb4cf2c8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SPIRONOLACTONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA089424
- Marketing category
- ANDA
- Marketing start
- 2020-06-05
- Marketing end
- 0000-00-00
- Substance
- SPIRONOLACTONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-1063 | SPIRONOLACTONE TABLET [BRYANT RANCH PREPACK] | 5 | Legacy NDC | 20231116_26a956c7-9437-408c-b491-20787fa01ce2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1063-1 | 63629106301 | 500 TABLET in 1 BOTTLE, PLASTIC (63629-1063-1) | 500 tablet | 2020-06-05 | 0000-00-00 | No | No | Current |