spironolactone
- Product NDC
- 70518-2386
- 11-digit product format
- 705182386
- Labeler code
- 70518
- Product ID
- 70518-2386_c8bc7f56-e133-491a-e053-2995a90a3890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205936
- Marketing category
- ANDA
- Marketing start
- 2019-10-24
- 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 |
|---|
| 70518-2386 | SPIRONOLACTONE TABLET [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250315_172a4282-cbbb-417d-98e3-1e9c6b136ef1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2386-0 | 70518238600 | 100 POUCH in 1 BOX, UNIT-DOSE (70518-2386-0) > 1 TABLET in 1 POUCH (70518-2386-1) | 100 pouch | 2019-10-24 | 0000-00-00 | No | No | Current |