What is NDC 71335-1481?

71335-1481 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 25 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-1481

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1481Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1481Add 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
71335-1481-0	7133514810071335148100	120 TABLET in 1 BOTTLE (71335-1481-0)Marketed from Mar 29, 2002
71335-1481-1	7133514810171335148101	100 TABLET in 1 BOTTLE (71335-1481-1)Marketed from Mar 29, 2002
71335-1481-2	7133514810271335148102	30 TABLET in 1 BOTTLE (71335-1481-2)Marketed from Mar 29, 2002
71335-1481-3	7133514810371335148103	7 TABLET in 1 BOTTLE (71335-1481-3)Marketed from Mar 29, 2002
71335-1481-4	7133514810471335148104	14 TABLET in 1 BOTTLE (71335-1481-4)Marketed from Mar 29, 2002
71335-1481-5	7133514810571335148105	60 TABLET in 1 BOTTLE (71335-1481-5)Marketed from Mar 29, 2002
71335-1481-6	7133514810671335148106	2 TABLET in 1 BOTTLE (71335-1481-6)Marketed from Mar 29, 2002
71335-1481-7	7133514810771335148107	90 TABLET in 1 BOTTLE (71335-1481-7)Marketed from Mar 29, 2002
71335-1481-8	7133514810871335148108	4 TABLET in 1 BOTTLE (71335-1481-8)Marketed from Mar 29, 2002
71335-1481-9	7133514810971335148109	8 TABLET in 1 BOTTLE (71335-1481-9)Marketed from Mar 29, 2002

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): Hydrochlorothiazide
Generic name (nonproprietary): hydrochlorothiazide
Active ingredients: Hydrochlorothiazide — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040412
Marketing start: Mar 29, 2002
Listing expires: Dec 31, 2026
Other FDA classes: Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 71335-1481_046b6751-595e-4fd5-96de-d5697238026fSPL ID 046b6751-595e-4fd5-96de-d5697238026fSPL set ID 0fdb6713-8013-4cfe-a776-0c1e9414a91cRxCUI 197770, 310798UNII 0J48LPH2TH
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

N471335148100 followed by a unit qualifier and the quantity

Package 71335-1481-00. 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 Jun 2, 2020.

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 71335-1481

What is NDC 71335-1481?: 71335-1481 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 25 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 040412

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

FDA NDC Directory listings under ANDA 040412
Product	Strength	Form · route	Labeler	Product NDC
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Solco Healthcare U.S., LLC	43547-397
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Solco Healthcare U.S., LLC	43547-398
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	American Health Packaging	60687-593
Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1	TabletOral	Bryant Ranch Prepack	63629-1218
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-1220
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-8992
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-1451
Hydrochlorothiazide	Hydrochlorothiazide 50 mg/1	TabletOral	Bryant Ranch Prepack	72162-1357