NDC codes

FDA NDC Directory
Product NDC (as listed)31722-701Labeler and product segments. Claims need a package NDC.
Product NDC at billing width31722-0701Add 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
31722-701-0531722070105500 TABLET, FILM COATED in 1 BOTTLE (31722-701-05)Marketed from Aug 19, 2015
31722-701-10317220701101000 TABLET, FILM COATED in 1 BOTTLE (31722-701-10)Marketed from Aug 19, 2015
31722-701-303172207013030 TABLET, FILM COATED in 1 BOTTLE (31722-701-30)Marketed from Aug 19, 2015
31722-701-603172207016060 TABLET, FILM COATED in 1 BOTTLE (31722-701-60)Marketed from Aug 19, 2015
31722-701-903172207019090 TABLET, FILM COATED in 1 BOTTLE (31722-701-90)Marketed from Aug 19, 2015

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
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 31722-701_40b34aeb-20b5-4200-e063-6394a90a96e9SPL ID 40b34aeb-20b5-4200-e063-6394a90a96e9SPL set ID cafd54e8-42a8-474c-8ea8-49ec74c2b0d3RxCUI 979480, 979485, 979492UNII 3ST302B24AUPC 0331722702300, 0331722700900, 0331722701303

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

N431722070105 followed by a unit qualifier and the quantity

Package 31722-0701-05. 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)

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 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2216
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7888
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4695
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralDirect_Rx72189-097
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralDIRECT RX72189-096
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4489
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4471
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5114
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-854
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 50 mg/1Tablet, Film coatedOralProficient Rx LP63187-296
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralProficient Rx LP63187-708
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4645
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5175
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-029
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5181
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-342
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-340
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-341

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Losartan Potassium NDC 31722-701 | Med-Code