NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2366Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2366Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71335-2366-17133523660130 TABLET in 1 BOTTLE, PLASTIC (71335-2366-1)Marketed from Apr 30, 2024
71335-2366-27133523660260 TABLET in 1 BOTTLE, PLASTIC (71335-2366-2)Marketed from Apr 30, 2024
71335-2366-37133523660390 TABLET in 1 BOTTLE, PLASTIC (71335-2366-3)Marketed from Apr 30, 2024
71335-2366-47133523660414 TABLET in 1 BOTTLE, PLASTIC (71335-2366-4)Marketed from Apr 30, 2024
71335-2366-571335236605100 TABLET in 1 BOTTLE, PLASTIC (71335-2366-5)Marketed from Apr 30, 2024
71335-2366-6713352366067 TABLET in 1 BOTTLE, PLASTIC (71335-2366-6)Marketed from Apr 30, 2024
71335-2366-77133523660710 TABLET in 1 BOTTLE, PLASTIC (71335-2366-7)Marketed from Apr 30, 2024
71335-2366-871335236608180 TABLET in 1 BOTTLE, PLASTIC (71335-2366-8)Marketed from Apr 30, 2024
71335-2366-97133523660945 TABLET in 1 BOTTLE, PLASTIC (71335-2366-9)Marketed from Apr 30, 2024

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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 089424
Marketing start
Listing expires
Other FDA classes
Aldosterone Antagonists (Mechanism)
Identifiers
Product ID 71335-2366_e91ce04a-ddcd-4a7b-b86a-73e9aabab7a8SPL ID e91ce04a-ddcd-4a7b-b86a-73e9aabab7a8SPL set ID ca194a2a-ed16-40f6-a78c-45c5f3392170RxCUI 313096UNII 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

N471335236601 followed by a unit qualifier and the quantity

Package 71335-2366-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Spironolactone tablets are an aldosterone antagonist indicated for: • The treatment of NYHA Class III-IV heart failure and reduced ejection fraction to increase survival, manage edema, and to reduce the need for hospitalization for heart failure ( 1.1 ). • Use as an add-on therapy for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions ( 1.2 ). • The management of edema in adult patients who are cirrhotic when edema is not responsive to fluid and sodium restrictions and in the setting of nephrotic syndrome when treatment of the underlying disease, restriction…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 089424

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

FDA NDC Directory listings under ANDA 089424
ProductStrengthForm · routeLabelerProduct NDC
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6408
SpironolactoneSpironolactone 25 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-143
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1065
SpironolactoneSpironolactone 25 mg/1TabletOralBryant Ranch Prepack63629-1061
SpironolactoneSpironolactone 25 mg/1TabletOralBryant Ranch Prepack63629-1062
SpironolactoneSpironolactone 25 mg/1TabletOralBryant Ranch Prepack63629-1064
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1066
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1067
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1092
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1094
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2887
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-4094
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.53489-328
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.53489-329
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6432
SpironolactoneSpironolactone 25 mg/1TabletOralBryant Ranch Prepack63629-8539
SpironolactoneSpironolactone 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-5341
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2204
SpironolactoneSpironolactone 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2203
SpironolactoneSpironolactone 25 mg/1TabletOralBryant Ranch Prepack71335-2205

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