What is NDC 0904-6927?

0904-6927 is the product NDC for spironolactone, Spironolactone 25 mg/1 tablet, film coated, listed with the FDA by Major Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.

Major Pharmaceuticals, NDC labeler code 0904. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for spironolactone?

177 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

spironolactone NDC 0904-6927 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0904-6927Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00904-6927Add 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 NDC	11-digit (billing)	Package	Copy
0904-6927-61	0090469276100904692761	100 BLISTER PACK in 1 CARTON (0904-6927-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Aug 15, 2018

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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: Major PharmaceuticalsNDC labeler code 0904
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205936
Marketing start: Aug 15, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Aldosterone Antagonists (Mechanism)
Identifiers: Product ID 0904-6927_c37ed479-700b-4d5c-b269-383f2d2f9fd5SPL ID c37ed479-700b-4d5c-b269-383f2d2f9fd5SPL set ID 0c45d793-6f2f-4622-b5ed-6875acfbc02bRxCUI 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

N400904692761 followed by a unit qualifier and the quantity

Package 00904-6927-61. 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 Oct 20, 2026.

Indications (excerpt from the label)

Spironolactone is 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 of fluid…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0904-6927

What is NDC 0904-6927?: 0904-6927 is the product NDC for spironolactone, Spironolactone 25 mg/1 tablet, film coated, listed with the FDA by Major Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: spironolactone.
What is the active ingredient?: Spironolactone.
Who is the labeler?: Major Pharmaceuticals, NDC labeler code 0904. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for spironolactone?: 177 other product NDCs are listed under this name. See all spironolactone NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other spironolactone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Spironolactone	Spironolactone 100 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4188	68788-4188-0368788-4188-0668788-4188-09
Spironolactone	Spironolactone 50 mg/1	Tablet, CoatedOral	Coupler LLC	67046-0613	67046-0613-03
Spironolactone	Spironolactone 25 mg/1	Tablet, CoatedOral	Coupler LLC	67046-0744	67046-0744-03
Spironolactone	Spironolactone 25 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-087	48433-0087-20
Spironolactone	Spironolactone 50 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-088	48433-0088-20
Spironolactone	Spironolactone 100 mg/1	Tablet, Film coatedOral	Safecor Health LLC	48433-089	48433-0089-08
Spironolactone	Spironolactone 100 mg/1	Tablet, CoatedOral	Coupler LLC	67046-1636	67046-1636-03
spironolactone	Spironolactone 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4512	70518-4512-0070518-4512-02
Spironolactone	Spironolactone 25 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-706	64980-0706-0164980-0706-50
Spironolactone	Spironolactone 50 mg/1	TabletOral	Rising Pharma Holdings, Inc.	64980-707	64980-0707-0164980-0707-50

All 178 spironolactone NDCs

Other NDCs under ANDA 205936

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

FDA NDC Directory listings under ANDA 205936
Product	Strength	Form · route	Labeler	Product NDC
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 50 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-861
spironolactone	Spironolactone 25 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-3556
Spironolactone	Spironolactone 25 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-465
Spironolactone	Spironolactone 50 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-476
Spironolactone	Spironolactone 100 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-487
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 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4468
spironolactone	Spironolactone 25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4470
spironolactone	Spironolactone 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4512
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 100 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1029