NDC codes

FDA NDC Directory
Product NDC (as listed)42799-920Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42799-0920Add 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
42799-920-0142799092001100 TABLET, FILM COATED in 1 BOTTLE (42799-920-01)Marketed from Apr 30, 2019
42799-920-0242799092002500 TABLET, FILM COATED in 1 BOTTLE (42799-920-02)Marketed from Apr 30, 2019
42799-920-304279909203030 TABLET, FILM COATED in 1 BOTTLE (42799-920-30)Marketed from Apr 30, 2019

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 and Hydrochlorothiazide
Generic name (nonproprietary)
bisoprolol fumarate and hydrochlorothiazide
Active ingredients
Bisoprolol fumarate2.5 mg/1Hydrochlorothiazide6.25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212678
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 42799-920_523ed43b-4b04-4a00-abd0-478f9afc646fSPL ID 523ed43b-4b04-4a00-abd0-478f9afc646fSPL set ID 295532b5-65c8-40c3-8d27-cfd334d12802RxCUI 854908, 854916, 854919UNII UR59KN573L, 0J48LPH2THUPC 0342799921020, 0342799920016, 0342799922010, 0342799920023, 0342799921013, 0342799920306, 0342799922300, 0342799922027, 0342799921303
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

N442799092001 followed by a unit qualifier and the quantity

Package 42799-0920-01. 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 & 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 212678

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

FDA NDC Directory listings under ANDA 212678
ProductStrengthForm · routeLabelerProduct NDC
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5905
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralEdenbridge Pharmaceuticals LLC.42799-921
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralEdenbridge Pharmaceuticals LLC.42799-922
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1931
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1769
Bisoprolol Fumarate and HydrochlorothiazideBisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5849

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