What is NDC 50419-542?

50419-542 is the product NDC for Finerenone, Finerenone 40 mg/1 tablet, listed with the FDA by Bayer HealthCare Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Bayer HealthCare Pharmaceuticals Inc., NDC labeler code 50419. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Finerenone?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Finerenone NDC 50419-542 | National Drug Code

Unfinished product

This listing is a drug for further processing, not a finished drug product dispensed or administered to patients. It is not normally billed.

NDC codes

FDA NDC Directory

Product NDC (as listed)50419-542Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50419-0542Add 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
50419-542-05	50419054205	10 BLISTER PACK in 1 CARTON (50419-542-05) / 10 TABLET in 1 BLISTER PACKMarketed from 13-JUL-25

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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

Generic name (nonproprietary): finerenone
Active ingredients: Finerenone — 40 mg/1
Dosage form: Tablet
Labeler: Bayer HealthCare Pharmaceuticals Inc.NDC labeler code 50419
Product type: Drug for further processing
Marketing category: Drug for further processing
Marketing start: Jul 13, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 50419-542_50f5445b-9439-4b9b-adfe-6a972d46b02cSPL ID 50f5445b-9439-4b9b-adfe-6a972d46b02c

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N450419054205 followed by a unit qualifier and the quantity

Package 50419-0542-05. 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.

About NDC 50419-542

What is NDC 50419-542?: 50419-542 is the product NDC for Finerenone, Finerenone 40 mg/1 tablet, listed with the FDA by Bayer HealthCare Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Finerenone.
What is the active ingredient?: Finerenone.
Who is the labeler?: Bayer HealthCare Pharmaceuticals Inc., NDC labeler code 50419. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Finerenone?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.