NDC codes

FDA NDC Directory
Product NDC (as listed)72888-092Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72888-0092Add 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
72888-092-00728880092001000 TABLET, FILM COATED in 1 BOTTLE (72888-092-00)Marketed from Jul 1, 2022
72888-092-0172888009201100 TABLET, FILM COATED in 1 BOTTLE (72888-092-01)Marketed from Jul 1, 2022
72888-092-0572888009205500 TABLET, FILM COATED in 1 BOTTLE (72888-092-05)Marketed from Jul 1, 2022
72888-092-307288800923030 TABLET, FILM COATED in 1 BOTTLE (72888-092-30)Marketed from Jul 1, 2022

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 Fumarate
Generic name (nonproprietary)
bisoprolol fumarate
Active ingredients
Bisoprolol fumarate — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075643
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 72888-092_43603823-594f-cbe7-e063-6294a90a9153SPL ID 43603823-594f-cbe7-e063-6294a90a9153SPL set ID 83e4b4e5-9130-44c8-abab-fcd0db5d8c49RxCUI 854901, 854905, 865155UNII UR59KN573LUPC 0372888093000, 0372888093055, 0372888092010, 0372888092003, 0372888093017, 0372888092058, 0372888233017, 0372888092300, 0372888093307
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

N472888009200 followed by a unit qualifier and the quantity

Package 72888-0092-00. 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

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)

Other NDCs under ANDA 075643

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

FDA NDC Directory listings under ANDA 075643
ProductStrengthForm · routeLabelerProduct NDC
Bisoprolol FumarateBisoprolol fumarate 2.5 mg/1Tablet, Film coatedOralTruPharma LLC52817-268
Bisoprolol FumarateBisoprolol fumarate 10 mg/1Tablet, Film coatedOralAdvagen Pharma Ltd72888-093
Bisoprolol FumarateBisoprolol fumarate 2.5 mg/1Tablet, Film coatedOralAdvagen Pharma Ltd72888-233
Bisoprolol FumarateBisoprolol fumarate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-9755

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