NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1373Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1373Add 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
70771-1373-17077113730170771137301100 TABLET in 1 BOTTLE (70771-1373-1)Marketed from Mar 12, 2019

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)
Atenolol and Chlorthalidone
Generic name (nonproprietary)
atenolol and chlorthalidone
Active ingredients
Atenolol — 100 mg/1Chlorthalidone — 25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210028
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)Increased Diuresis (Physiologic effect)
Identifiers
Product ID 70771-1373_743d8c46-3adb-4e47-bdc6-68f4fd1f34fbSPL ID 743d8c46-3adb-4e47-bdc6-68f4fd1f34fb
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

N470771137301 followed by a unit qualifier and the quantity

Package 70771-1373-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70771-1373

What is NDC 70771-1373?
70771-1373 is the product NDC for Atenolol and Chlorthalidone, Atenolol 100 mg/1; Chlorthalidone 25 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Atenolol and Chlorthalidone.
What is the active ingredient?
Atenolol, Chlorthalidone.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Atenolol and Chlorthalidone?
15 other product NDCs are listed under this name. See all Atenolol and Chlorthalidone NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Atenolol and Chlorthalidone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-415668788-4156-01
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralREMEDYREPACK INC.70518-411170518-4111-00
Atenolol And Chlorthalidoneatenolol and chlorthalidone tabletChlorthalidone 25 mg/1; Atenolol 50 mg/1TabletOralMARLEX PHARMACEUTICALS, INC10135-73310135-0733-01
Atenolol And Chlorthalidoneatenolol and chlorthalidone tabletAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralMARLEX PHARMACEUTICALS, INC10135-73410135-0734-01
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralANI Pharmaceuticals, Inc.70954-39070954-0390-10
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralANI Pharmaceuticals, Inc.70954-39170954-0391-10
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-40029300-0400-0129300-0400-05
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-40129300-0401-0129300-0401-05
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralNorthstar Rx LLC.16714-93616714-0936-01
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralNorthstar Rx LLC.16714-93716714-0937-01

All 16 Atenolol and Chlorthalidone NDCs

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
ProductStrengthForm · routeLabelerProduct NDC
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralNorthstar Rx LLC.16714-936
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralNorthstar Rx LLC.16714-937
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1167
Atenolol and ChlorthalidoneAtenolol 100 mg/1; Chlorthalidone 25 mg/1TabletOralZydus Pharmaceuticals USA Inc.70710-1168
Atenolol and ChlorthalidoneAtenolol 50 mg/1; Chlorthalidone 25 mg/1TabletOralZydus Lifesciences Limited70771-1372

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