NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6908Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6908Add 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
50090-6908-050090690800100 TABLET in 1 BOTTLE (50090-6908-0)Marketed from Dec 12, 2023
50090-6908-15009069080130 TABLET in 1 BOTTLE (50090-6908-1)Marketed from Dec 12, 2023
50090-6908-65009069080690 TABLET in 1 BOTTLE (50090-6908-6)Marketed from Dec 12, 2023

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 202187
Marketing start
Listing expires
Other FDA classes
Aldosterone Antagonists (Mechanism)
Identifiers
Product ID 50090-6908_b8981ce7-0475-490c-9035-71717a62124cSPL ID b8981ce7-0475-490c-9035-71717a62124cSPL set ID 7ef0c2bb-9657-419e-848c-858893be50bcRxCUI 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

N450090690800 followed by a unit qualifier and the quantity

Package 50090-6908-00. 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

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

Other NDCs under ANDA 202187

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

FDA NDC Directory listings under ANDA 202187
ProductStrengthForm · routeLabelerProduct NDC
SpironolactoneSpironolactone 50 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3795
SpironolactoneSpironolactone 25 mg/1TabletOralRedpharm Drug67296-2319
SpironolactoneSpironolactone 100 mg/1TabletOralREMEDYREPACK INC.70518-4447
SpironolactoneSpironolactone 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2989
SpironolactoneSpironolactone 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2988
SpironolactoneSpironolactone 100 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3903
SpironolactoneSpironolactone 50 mg/1TabletOralA-S Medication Solutions50090-7082
SpironolactoneSpironolactone 50 mg/1TabletOralA-S Medication Solutions50090-7083
SpironolactoneSpironolactone 50 mg/1TabletOralAurobindo Pharma Limited59651-427
SpironolactoneSpironolactone 25 mg/1TabletOralAurobindo Pharma Limited59651-426
SpironolactoneSpironolactone 100 mg/1TabletOralAurobindo Pharma Limited59651-428
SpironolactoneSpironolactone 25 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8451
SpironolactoneSpironolactone 50 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8452
SpironolactoneSpironolactone 100 mg/1TabletOralNorthStar Rx LLC72603-136
SpironolactoneSpironolactone 25 mg/1TabletOralNorthStar Rx LLC72603-134
SpironolactoneSpironolactone 50 mg/1TabletOralNorthStar Rx LLC72603-135
SpironolactoneSpironolactone 50 mg/1TabletOralRedpharm Drug67296-2285
SpironolactoneSpironolactone 25 mg/1TabletOralA-S Medication Solutions50090-6909

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