NDC codes

FDA NDC Directory
Product NDC (as listed)82804-317Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0317Add 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
82804-317-30828040317308280403173030 TABLET in 1 BOTTLE (82804-317-30)Marketed from Sep 23, 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 — 25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 82804
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213412
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)
Identifiers
Product ID 82804-317_73db0625-00f2-4fc9-9095-c64bccdda33dSPL ID 73db0625-00f2-4fc9-9095-c64bccdda33d
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

N482804031730 followed by a unit qualifier and the quantity

Package 82804-0317-30. 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 82804-317

What is NDC 82804-317?
82804-317 is the product NDC for Chlorthalidone, Chlorthalidone 25 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 1 package NDC, 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?
Proficient Rx LP, NDC labeler code 82804. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ChlorthalidoneChlorthalidone 25 mg/1TabletOralIpca Laboratories Limited83980-06183980-0061-0183980-0061-1083980-0061-13+2 more
ChlorthalidoneChlorthalidone 50 mg/1TabletOralIpca Laboratories Limited83980-06283980-0062-0183980-0062-1083980-0062-13+1 more
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416968788-4169-0368788-4169-09
ChlorthalidoneChlorthalidone 25 mg/1TabletOralMacleods Pharmaceuticals Limited33342-42533342-0425-0733342-0425-1033342-0425-11+1 more
ChlorthalidoneChlorthalidone 50 mg/1TabletOralMacleods Pharmaceuticals Limited33342-42633342-0426-0733342-0426-1033342-0426-11+1 more
ChlorthalidoneChlorthalidone 25 mg/1TabletOralSafecor Health, LLC48433-02148433-0021-20
ChlorthalidoneChlorthalidone 25 mg/1TabletOralREMEDYREPACK INC.70518-457870518-4578-00
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-407768788-4077-0368788-4077-09
ChlorthalidoneChlorthalidone 25 mg/1TabletOralUmedica Laboratories USA Inc.60290-00460290-0004-0160290-0004-02
ChlorthalidoneChlorthalidone 50 mg/1TabletOralUmedica Laboratories USA Inc.60290-00560290-0005-0160290-0005-02

All 99 Chlorthalidone NDCs

Other NDCs under ANDA 213412

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

FDA NDC Directory listings under ANDA 213412
ProductStrengthForm · routeLabelerProduct NDC
ChlorthalidoneChlorthalidone 50 mg/1TabletOralA-S Medication Solutions50090-5183
ChlorthalidoneChlorthalidone 25 mg/1TabletOralA-S Medication Solutions50090-6126
ChlorthalidoneChlorthalidone 25 mg/1TabletOralA-S Medication Solutions50090-7831
ChlorthalidoneChlorthalidone 25 mg/1TabletOralBryant Ranch Prepack63629-8761
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack63629-8762
ChlorthalidoneChlorthalidone 50 mg/1TabletOralCoupler LLC67046-1499
ChlorthalidoneChlorthalidone 25 mg/1TabletOralAscend Laboratories, LLC67877-696
ChlorthalidoneChlorthalidone 50 mg/1TabletOralAscend Laboratories, LLC67877-697
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4053
ChlorthalidoneChlorthalidone 25 mg/1TabletOralREMEDYREPACK INC.70518-3954
ChlorthalidoneChlorthalidone 25 mg/1TabletOralBryant Ranch Prepack71335-2072
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack71335-2580
ChlorthalidoneChlorthalidone 25 mg/1TabletOralDirect_Rx72189-644

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in