Spironolactone
- Product NDC
- 70518-0603
- 11-digit product format
- 705180603
- Labeler code
- 70518
- Product ID
- 70518-0603_e1f9f691-e0d4-a098-e053-2a95a90a9184
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- spironolactone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203253
- Marketing category
- ANDA
- Marketing start
- 2017-06-29
- 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
- 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 |
|---|
| 70518-0603-1 | 70518060301 | 100 POUCH in 1 BOX (70518-0603-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0603-2) | 100 pouch | 2021-12-02 | 0000-00-00 | No | No | Current |