Prescription drug · ANDA
Bisoprolol Fumarate and Hydrochlorothiazide NDC 42799-920
Bisoprolol fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film coated · Oral · Edenbridge Pharmaceuticals LLC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 42799-920-01 | 42799092001 | 100 TABLET, FILM COATED in 1 BOTTLE (42799-920-01)Marketed from Apr 30, 2019 | |
| 42799-920-02 | 42799092002 | 500 TABLET, FILM COATED in 1 BOTTLE (42799-920-02)Marketed from Apr 30, 2019 | |
| 42799-920-30 | 42799092030 | 30 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 fumarate — 2.5 mg/1Hydrochlorothiazide — 6.25 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
N442799092001followed by a unit qualifier and the quantityPackage 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.
Other NDCs under ANDA 212678
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-5905 |
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | Edenbridge Pharmaceuticals LLC. | 42799-921 |
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 10 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | Edenbridge Pharmaceuticals LLC. | 42799-922 |
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1931 |
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1769 |
| Bisoprolol Fumarate and Hydrochlorothiazide | Bisoprolol fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-5849 |
- openFDA data updated
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