NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6413Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6413Add 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
50090-6413-05009064130030 TABLET in 1 BOTTLE (50090-6413-0)Marketed from Mar 28, 2023
50090-6413-25009064130290 TABLET in 1 BOTTLE (50090-6413-2)Marketed from Mar 28, 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 and Hydrochlorothiazide
Generic name (nonproprietary)
bisoprolol fumarate and hydrochlorothiazide
Active ingredients
Bisoprolol fumarate — 5 mg/1Hydrochlorothiazide — 6.25 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215562
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 50090-6413_b4dbad3e-db70-448f-8946-c9a2ae7bec87SPL ID b4dbad3e-db70-448f-8946-c9a2ae7bec87SPL set ID 90bb2207-2eaf-495b-a222-c69d4db9e7a3RxCUI 854919UNII UR59KN573L, 0J48LPH2TH
Pharmacologic class
Thiazide Diuretic; 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

N450090641300 followed by a unit qualifier and the quantity

Package 50090-6413-00. 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 & USAGE Bisoprolol fumarate and hydrochlorothiazide tablets are indicated in the management of hypertension.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 215562

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

FDA NDC Directory listings under ANDA 215562
ProductStrengthForm · routeLabelerProduct NDC
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-741
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralANI Pharmaceuticals, Inc.70954-412
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralANI Pharmaceuticals, Inc.70954-413
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralANI Pharmaceuticals, Inc.70954-414
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-740
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-742

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