Spironolactone NDC 68788-4188

Product information

Brand name (proprietary)

Spironolactone

Generic name (nonproprietary)

spironolactone

Active ingredients

Spironolactone — 100 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Preferred Pharmaceuticals Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 089424

Marketing start

Aug 27, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Aldosterone Antagonists (Mechanism)

Identifiers

Product ID 68788-4188_3486d831-06b6-4e8f-bd6f-52f7759988f5SPL ID 3486d831-06b6-4e8f-bd6f-52f7759988f5SPL set ID 3486d831-06b6-4e8f-bd6f-52f7759988f5RxCUI 198222UNII 27O7W4T232

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

N468788418803 followed by a unit qualifier and the quantity Copy

Package 68788-4188-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 089424

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

Showing 20 of 38.