What is NDC 83980-062?

83980-062 is the product NDC for Chlorthalidone, Chlorthalidone 50 mg/1 tablet, listed with the FDA by Ipca Laboratories Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

Ipca Laboratories Limited, NDC labeler code 83980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Chlorthalidone?

98 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlorthalidone NDC 83980-062 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)83980-062Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83980-0062Add 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
83980-062-01	8398000620183980006201	100 TABLET in 1 BOTTLE (83980-062-01)Marketed from Sep 21, 2026
83980-062-10	8398000621083980006210	1000 TABLET in 1 BOTTLE (83980-062-10)Marketed from Sep 21, 2026
83980-062-13	8398000621383980006213	30 TABLET in 1 BOTTLE (83980-062-13)Marketed from Sep 21, 2026
83980-062-19	8398000621983980006219	90 TABLET in 1 BOTTLE (83980-062-19)Marketed from Sep 21, 2026

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): Chlorthalidone
Generic name (nonproprietary): chlorthalidone
Active ingredients: Chlorthalidone — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Ipca Laboratories LimitedNDC labeler code 83980
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209162
Marketing start: Sep 21, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis (Physiologic effect)
Identifiers: Product ID 83980-062_b1a9b0ed-396f-41cc-b975-349b61b99d14SPL ID b1a9b0ed-396f-41cc-b975-349b61b99d14
Pharmacologic class: Thiazide-like Diuretic

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

N483980006201 followed by a unit qualifier and the quantity

Package 83980-0062-01. 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 83980-062

What is NDC 83980-062?: 83980-062 is the product NDC for Chlorthalidone, Chlorthalidone 50 mg/1 tablet, listed with the FDA by Ipca Laboratories Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chlorthalidone.
What is the active ingredient?: Chlorthalidone.
Who is the labeler?: Ipca Laboratories Limited, NDC labeler code 83980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chlorthalidone?: 98 other product NDCs are listed under this name. See all 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 Chlorthalidone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Ipca Laboratories Limited	83980-061	83980-0061-0183980-0061-1083980-0061-13+2 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4169	68788-4169-0368788-4169-09
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-426	33342-0426-0733342-0426-1033342-0426-11+1 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-425	33342-0425-0733342-0425-1033342-0425-11+1 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Safecor Health, LLC	48433-021	48433-0021-20
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4578	70518-4578-00
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4077	68788-4077-0368788-4077-09
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-004	60290-0004-0160290-0004-02
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-005	60290-0005-0160290-0005-02
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Major Pharmaceuticals	0904-7583	00904-7583-0400904-7583-61

All 99 Chlorthalidone NDCs

Other NDCs under ANDA 209162

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

FDA NDC Directory listings under ANDA 209162
Product	Strength	Form · route	Labeler	Product NDC
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Ipca Laboratories Limited	83980-061