NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2244Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2244Add 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
71335-2244-17133522440130 TABLET in 1 BOTTLE, PLASTIC (71335-2244-1)Marketed from Sep 22, 2023
71335-2244-271335224402120 TABLET in 1 BOTTLE, PLASTIC (71335-2244-2)Marketed from Sep 22, 2023
71335-2244-371335224403180 TABLET in 1 BOTTLE, PLASTIC (71335-2244-3)Marketed from Sep 22, 2023
71335-2244-47133522440490 TABLET in 1 BOTTLE, PLASTIC (71335-2244-4)Marketed from Sep 22, 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)
Bisoprolol Fumarate
Generic name (nonproprietary)
bisoprolol fumarate
Active ingredients
Bisoprolol fumarate — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078635
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 71335-2244_b77f45b2-ce63-417b-abdb-e6f807c1ec6cSPL ID b77f45b2-ce63-417b-abdb-e6f807c1ec6cSPL set ID 4f11e64c-732e-419a-bc29-9cd2ff86d0b9RxCUI 854901UNII UR59KN573L
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

N471335224401 followed by a unit qualifier and the quantity

Package 71335-2244-01. 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 is 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)

Other NDCs under ANDA 078635

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

FDA NDC Directory listings under ANDA 078635
ProductStrengthForm · routeLabelerProduct NDC
Bisoprolol FumarateBisoprolol fumarate 10 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-127
Bisoprolol FumarateBisoprolol fumarate 5 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-126
Bisoprolol FumarateBisoprolol fumarate 5 mg/1TabletOralBryant Ranch Prepack63629-5173
Bisoprolol FumarateBisoprolol fumarate 5 mg/1TabletOralAmerican Health Packaging60687-679
Bisoprolol FumarateBisoprolol fumarate 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8671
Bisoprolol FumarateBisoprolol fumarate 5 mg/1TabletOralProficient Rx LP63187-871

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