NDC codes

FDA NDC Directory
Product NDC (as listed)42571-471Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42571-0471Add 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
42571-471-014257104710142571047101100 TABLET, FILM COATED in 1 BOTTLE (42571-471-01)Marketed from Jun 1, 2026
42571-471-054257104710542571047105500 TABLET, FILM COATED in 1 BOTTLE (42571-471-05)Marketed from Jun 1, 2026
42571-471-30425710471304257104713030 TABLET, FILM COATED in 1 BOTTLE (42571-471-30)Marketed from Jun 1, 2026

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

Brand name (proprietary)
Bisoprolol
Generic name (nonproprietary)
bisoprolol fumarate
Active ingredients
Bisoprolol fumarate — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Micro Labs LimitedNDC labeler code 42571
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218303
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 42571-471_4cbe74e3-3af3-2b98-e063-6294a90a1c2bSPL ID 4cbe74e3-3af3-2b98-e063-6294a90a1c2bSPL set ID c3ee566c-74c4-45f4-a947-526a7313e326RxCUI 854901, 854905UNII UR59KN573LUPC 0342571470302, 0342571471309
Pharmacologic class
beta-Adrenergic Blocker

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

N442571047101 followed by a unit qualifier and the quantity

Package 42571-0471-01. 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)

INDICATIONS AND USAGE Bisoprolol fumarate tablets are indicated in the management of hypertension. It may be used alone or in combination with other antihypertensive agents.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 42571-471

What is NDC 42571-471?
42571-471 is the product NDC for Bisoprolol (bisoprolol fumarate), Bisoprolol fumarate 10 mg/1 tablet, film coated, listed with the FDA by Micro Labs Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bisoprolol (Bisoprolol fumarate).
What is the active ingredient?
Bisoprolol fumarate.
Who is the labeler?
Micro Labs Limited, NDC labeler code 42571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bisoprolol?
6 other product NDCs are listed under this name. See all Bisoprolol 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 Bisoprolol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Bisoprololbisoprolol fumarateBisoprolol fumarate 5 mg/1Tablet, Film coatedOralMicro Labs Limited42571-47042571-0470-0142571-0470-0542571-0470-30
Bisoprololbisoprolol fumarateBisoprolol fumarate 5 mg/1Tablet, Film coatedOralTruPharma, LLC52817-27052817-0270-1052817-0270-30
Bisoprololbisoprolol fumarateBisoprolol fumarate 10 mg/1Tablet, Film coatedOralTruPharma, LLC52817-27152817-0271-1052817-0271-30
Bisoprololbisoprolol fumarateBisoprolol fumarate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-690763629-6907-0163629-6907-0263629-6907-03+1 more
Bisoprololbisoprolol fumarateBisoprolol fumarate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-167871335-1678-0171335-1678-0271335-1678-03+2 more
Bisoprololbisoprolol fumarateBisoprolol fumarate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-217772162-2177-01

Other NDCs under ANDA 218303

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

FDA NDC Directory listings under ANDA 218303
ProductStrengthForm · routeLabelerProduct NDC
Bisoprololbisoprolol fumarateBisoprolol fumarate 5 mg/1Tablet, Film coatedOralMicro Labs Limited42571-470

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