Atenolol and Chlorthalidone NDC 16714-937

NDC codes

FDA NDC Directory

Product NDC (as listed)16714-937Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16714-0937Add 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 NDC	11-digit (billing)	Package	Copy
16714-937-01	16714093701	100 TABLET in 1 BOTTLE (16714-937-01)Marketed from Mar 26, 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): Atenolol and Chlorthalidone
Generic name (nonproprietary): atenolol and chlorthalidone
Active ingredients: Atenolol — 100 mg/1Chlorthalidone — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Northstar Rx LLC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210028
Marketing start: Mar 26, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)Increased Diuresis (Physiologic effect)
Identifiers: Product ID 16714-937_8ca5026f-56b1-4f46-96f0-a36ace459fb5SPL ID 8ca5026f-56b1-4f46-96f0-a36ace459fb5SPL set ID 1494d5f7-8620-46da-8bca-69b76cd17635RxCUI 197382, 197383UNII Q0MQD1073Q, 50VV3VW0TI
Pharmacologic class: Thiazide-like 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

N416714093701 followed by a unit qualifier and the quantity

Package 16714-0937-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 210028

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

FDA NDC Directory listings under ANDA 210028
Product	Strength	Form · route	Labeler	Product NDC
Atenolol and Chlorthalidone	Atenolol 100 mg/1; Chlorthalidone 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1168
Atenolol and Chlorthalidone	Atenolol 50 mg/1; Chlorthalidone 25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1167
Atenolol and Chlorthalidone	Atenolol 50 mg/1; Chlorthalidone 25 mg/1	TabletOral	Northstar Rx LLC.	16714-936
Atenolol and Chlorthalidone	Atenolol 50 mg/1; Chlorthalidone 25 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1372
Atenolol and Chlorthalidone	Atenolol 100 mg/1; Chlorthalidone 25 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1373