NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1102Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1102Add 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
71335-1102-17133511020130 TABLET, FILM COATED in 1 BOTTLE (71335-1102-1)Marketed from Mar 16, 2016
71335-1102-27133511020290 TABLET, FILM COATED in 1 BOTTLE (71335-1102-2)Marketed from Mar 16, 2016
71335-1102-37133511020360 TABLET, FILM COATED in 1 BOTTLE (71335-1102-3)Marketed from Mar 16, 2016
71335-1102-471335110204120 TABLET, FILM COATED in 1 BOTTLE (71335-1102-4)Marketed from Mar 16, 2016
71335-1102-571335110205100 TABLET, FILM COATED in 1 BOTTLE (71335-1102-5)Marketed from Mar 16, 2016
71335-1102-671335110206180 TABLET, FILM COATED in 1 BOTTLE (71335-1102-6)Marketed from Mar 16, 2016
71335-1102-77133511020710 TABLET, FILM COATED in 1 BOTTLE (71335-1102-7)Marketed from Mar 16, 2016
71335-1102-8713351102087 TABLET, FILM COATED in 1 BOTTLE (71335-1102-8)Marketed from Mar 16, 2016

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 203835
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 71335-1102_48d9fcb2-155b-4f36-9cca-eb5f7d0a00a3SPL ID 48d9fcb2-155b-4f36-9cca-eb5f7d0a00a3SPL set ID 0f3a6984-e601-4a74-9910-49ee5e352d6bRxCUI 979480, 979485, 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

N471335110201 followed by a unit qualifier and the quantity

Package 71335-1102-01. 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 tablets are 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 t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1102

What is NDC 71335-1102?
71335-1102 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 8 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?
169 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 PotassiumlosartanLosartan potassium 50 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416068788-4160-0368788-4160-09
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-469570518-4695-00
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
Losartan PotassiumLosartan potassium 25 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-10011788-0100-1011788-0100-3011788-0100-90
Losartan PotassiumLosartan potassium 50 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-10111788-0101-1011788-0101-3011788-0101-90

All 170 Losartan Potassium NDCs

Other NDCs under ANDA 203835

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

FDA NDC Directory listings under ANDA 203835
ProductStrengthForm · routeLabelerProduct NDC
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-700
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-701
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-702
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralQPharma, Inc.42708-113
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralQPharma, Inc.42708-151
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralQPharma, Inc.42708-152
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-854
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4489
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4645
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4712
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4910
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4914
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7794
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7795
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7888
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7945
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7946
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-828
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-786
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralProficient Rx LP63187-296

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