Spironolactone
- Product NDC
- 50090-3580
- 11-digit product format
- 500903580
- Labeler code
- 50090
- Product ID
- 50090-3580_3f6adffa-ba58-469f-9e1a-720771a208df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203512
- Marketing category
- ANDA
- Marketing start
- 2017-06-02
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3580 | SPIRONOLACTONE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 13 | Legacy NDC | 20230524_1327c962-3302-4da2-b4c3-700e7c4d9d9c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3580-0 | 50090358000 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3580-0) | 2017-06-02 | 0000-00-00 | No | No | Current |
| 50090-3580-1 | 50090358001 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3580-1) | 2018-09-19 | 0000-00-00 | No | No | Current |
| 50090-3580-2 | 50090358002 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3580-2) | 2017-06-02 | 0000-00-00 | No | No | Current |