What is NDC 72789-303?

72789-303 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 50 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hydrochlorothiazide?

166 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Hydrochlorothiazide NDC 72789-303 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72789-303Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72789-0303Add 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
72789-303-01	7278903030172789030301	100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)Marketed from Mar 2, 2022

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): Hydrochlorothiazide
Generic name (nonproprietary): hydrochlorothiazide
Active ingredients: Hydrochlorothiazide — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040907
Marketing start: Aug 15, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 72789-303_3cf6edf5-e1bb-570f-e063-6294a90af580SPL ID 3cf6edf5-e1bb-570f-e063-6294a90af580SPL set ID 67bedecc-f758-4bc6-82c5-7d428cbbbd9bRxCUI 197770UNII 0J48LPH2THUPC 0372789303017
Pharmacologic class: Thiazide 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

N472789030301 followed by a unit qualifier and the quantity

Package 72789-0303-01. 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 Oct 27, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide tablets have also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Hydrochlorothiazide tablets are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension. Use in Pregnancy Routine use of diuretics during normal pregnancy is inappropriate and exposes m…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72789-303

What is NDC 72789-303?: 72789-303 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 50 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hydrochlorothiazide.
What is the active ingredient?: Hydrochlorothiazide.
Who is the labeler?: PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydrochlorothiazide?: 166 other product NDCs are listed under this name. See all Hydrochlorothiazide 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 Hydrochlorothiazide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/5mL	SolutionOral	Advagen Pharma Ltd	72888-491	72888-0491-01
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-3444	00480-3444-10
hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	CapsuleOral	Preferred Pharmaceuticals Inc.	68788-4192	68788-4192-0168788-4192-0368788-4192-06+2 more
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4736	70518-4736-00
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-038	87441-0038-01
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	Coupler LLC	67046-1664	67046-1664-03
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	American Health Packaging	60687-894	60687-0894-01
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-4525	70518-4525-00
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4466	70518-4466-0070518-4466-01
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4359	70518-4359-0070518-4359-0170518-4359-02+2 more

All 167 Hydrochlorothiazide NDCs

Other NDCs under ANDA 040907

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

FDA NDC Directory listings under ANDA 040907
Product	Strength	Form · route	Labeler	Product NDC
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-128
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-129
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-485
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	QPharma, Inc.	42708-079
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	A-S Medication Solutions	50090-0140
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	A-S Medication Solutions	50090-0141
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	A-S Medication Solutions	50090-5057
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Northwind Health Company, LLC	51655-422
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Lake Erie Medical DBA Quality Care Products LLC	55700-006
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	American Health Packaging	60687-894
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-315
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	Coupler LLC	67046-1664
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Redpharm drug	67296-2043
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4933
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8517
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3749
Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4736
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Proficient Rx LP	71205-419
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Bryant Ranch Prepack	71335-0652
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-1976

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