NDC codes

FDA NDC Directory
Product NDC (as listed)68382-136Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68382-0136Add 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
68382-136-016838201360168382013601100 TABLET, FILM COATED in 1 BOTTLE (68382-136-01)Marketed from Oct 4, 2010
68382-136-06683820136066838201360630 TABLET, FILM COATED in 1 BOTTLE (68382-136-06)Marketed from Oct 4, 2010
68382-136-1068382013610683820136101000 TABLET, FILM COATED in 1 BOTTLE (68382-136-10)Marketed from Oct 4, 2010
68382-136-16683820136166838201361690 TABLET, FILM COATED in 1 BOTTLE (68382-136-16)Marketed from Oct 4, 2010
68382-136-24683820136246838201362410000 TABLET, FILM COATED in 1 BOTTLE (68382-136-24)Marketed from Oct 4, 2010

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)
Losartan Potassium
Generic name (nonproprietary)
losartan potassium
Active ingredients
Losartan potassium — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Zydus Pharmaceuticals USA Inc.NDC labeler code 68382
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078243
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68382-136_cfd7f3a9-7719-43af-b0b4-f655824cb19bSPL ID cfd7f3a9-7719-43af-b0b4-f655824cb19bSPL set ID 3233c707-70b6-4c29-8210-913eeb2a38edRxCUI 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

N468382013601 followed by a unit qualifier and the quantity

Package 68382-0136-01. 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 tablets…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68382-136

What is NDC 68382-136?
68382-136 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 5 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?
Zydus Pharmaceuticals USA Inc., NDC labeler code 68382. 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 078243

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

FDA NDC Directory listings under ANDA 078243
ProductStrengthForm · routeLabelerProduct NDC
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-4783
Losortan Potassiumlosartan potassiumLosartan potassium 50 mg/1Tablet, Film coatedOralProficient Rx LP63187-071
Losortan Potassiumlosartan potassiumLosartan potassium 100 mg/1Tablet, Film coatedOralProficient Rx LP63187-072
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2089
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7958
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-135
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-137
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7959
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2326
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2327
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2333
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-6643
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7960
Losortan Potassiumlosartan potassiumLosartan potassium 25 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1644
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-731
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-729
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralZydus Lifesciences Limited65841-730
Losortan Potassiumlosartan potassiumLosartan potassium 100 mg/1Tablet, Film coatedOralAvPAK50268-506
Losortan Potassiumlosartan potassiumLosartan potassium 25 mg/1Tablet, Film coatedOralAvPAK50268-504
Losortan Potassiumlosartan potassiumLosartan potassium 50 mg/1Tablet, Film coatedOralAvPAK50268-505

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