NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0262Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0262Add 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
71335-0262-1713350262017133502620130 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1)Marketed from Apr 22, 2019
71335-0262-2713350262027133502620290 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2)Marketed from Apr 3, 2019
71335-0262-3713350262037133502620360 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3)Marketed from Jan 20, 2022
71335-0262-47133502620471335026204120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4)Marketed from Jan 20, 2022
71335-0262-57133502620571335026205100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5)Marketed from Jan 20, 2022
71335-0262-67133502620671335026206180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6)Marketed from Jan 20, 2022
71335-0262-7713350262077133502620710 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7)Marketed from Jan 20, 2022

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)
Losartan Potassium
Generic name (nonproprietary)
losartan potassium
Active ingredients
Losartan potassium — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091497
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 71335-0262_570fae9a-6e7f-4704-8ca0-12aa2e12f3e0SPL ID 570fae9a-6e7f-4704-8ca0-12aa2e12f3e0SPL set ID 43fa4762-cc0c-4a3b-a527-6aa7fb7c5464RxCUI 979492UNII 3ST302B24A

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

N471335026201 followed by a unit qualifier and the quantity

Package 71335-0262-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Losartan potassium is an angiotensin II receptor blocker (ARB) indicated for: • Treatment of hypertension, to lower blood pressure in adults and children greater than 6 years old. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) • Reduction of the risk of stroke in patients with hypertension and left ventricular hypertrophy. There is evidence that this benefit does not apply to Black patients. ( 1.2 ) • Treatment of diabetic nephropathy with an elevated serum creatinine and proteinuria in patients with type 2 diabetes and a history of hypertension. ( 1.3 ) 1.1 Hypertension Losartan potassium tablets ar…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0262

What is NDC 71335-0262?
71335-0262 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Losartan Potassium.
What is the active ingredient?
Losartan potassium.
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 Losartan Potassium?
173 other product NDCs are listed under this name. See all Losartan Potassium 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 Losartan Potassium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Losartan potassiumLosartan potassium 50 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-87660760-0876-30
Losartan potassiumLosartan potassium 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-477370518-4773-00
Losartan PotassiumlosartanLosartan potassium 50 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416068788-4160-0368788-4160-09
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-469570518-4695-0070518-4695-01
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-05287441-0052-01
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-05387441-0053-01
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralCoupler LLC67046-070267046-0702-03
Losartan potassiumLosartan potassium 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-412768788-4127-0368788-4127-09
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralCoupler LLC67046-108867046-1088-03
Losartan potassiumLosartan potassium 25 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-409168788-4091-0368788-4091-09

All 174 Losartan Potassium NDCs

Other NDCs under ANDA 091497

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

FDA NDC Directory listings under ANDA 091497
ProductStrengthForm · routeLabelerProduct NDC
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralSolco Healthcare US, LLC43547-360
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralSolco Healthcare US, LLC43547-361
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralSolco Healthcare US, LLC43547-362
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralProficient Rx LP63187-808
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralProficient Rx LP63187-830
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralCoupler LLC67046-1088
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,iNc.68071-1517
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2690
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals.Inc.68071-3846
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-4007
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8186
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8189
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3489
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralProficient Rx LP71205-226
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2083
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-207
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-224
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralDIRECT RX72189-100
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-052

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