Prescription drug · ANDA
spironolactone NDC 70518-4470
Spironolactone 25 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4470-0 | 70518447000 | 100 POUCH in 1 BOX (70518-4470-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4470-1)Marketed from Sep 8, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- spironolactone
- Generic name (nonproprietary)
- spironolactone
- Active ingredients
- Spironolactone — 25 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 205936
- Marketing start
- Listing expires
- Other FDA classes
- Aldosterone Antagonists (Mechanism)
- Identifiers
- Product ID 70518-4470_5b38b3cd-9301-e346-e063-6294a90ab713SPL ID 5b38b3cd-9301-e346-e063-6294a90ab713
- Pharmacologic class
- Aldosterone Antagonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470518447000followed by a unit qualifier and the quantityPackage 70518-4470-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
The FDA listing for this product does not reference a label (SPL) set.
Other NDCs under ANDA 205936
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| spironolactone | Spironolactone 50 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-861 |
| spironolactone | Spironolactone 100 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1029 |
| spironolactone | Spironolactone 25 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1027 |
| spironolactone | Spironolactone 50 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1028 |
| Spironolactone | Spironolactone 50 mg/1 | TabletOral | American Health Packaging | 60687-476 |
| Spironolactone | Spironolactone 100 mg/1 | TabletOral | American Health Packaging | 60687-487 |
| spironolactone | Spironolactone 50 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4468 |
| spironolactone | Spironolactone 25 mg/1 | Tablet, Film coatedOral | Cardinal Health 107, LLC | 55154-3556 |
| spironolactone | Spironolactone 100 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4512 |
| spironolactone | Spironolactone 25 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals (USA) Inc. | 68382-660 |
| spironolactone | Spironolactone 50 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals (USA) Inc. | 68382-661 |
| spironolactone | Spironolactone 100 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals (USA) Inc. | 68382-662 |
| spironolactone | Spironolactone 100 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-153 |
| spironolactone | Spironolactone 25 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-636 |
| spironolactone | Spironolactone 25 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | 0904-6927 |
| Spironolactone | Spironolactone 25 mg/1 | TabletOral | American Health Packaging | 60687-465 |