NDC codes

FDA NDC Directory
Product NDC (as listed)53401-029Labeler and product segments. Claims need a package NDC.
Product NDC at billing width53401-0029Add 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
53401-029-81534010029811080 TABLET in 1 BOTTLE (53401-029-81)Marketed from Aug 24, 2026

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)
Valsartan
Generic name (nonproprietary)
valsartan
Active ingredients
Valsartan — 80 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204011
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 53401-029_59d3da9b-42dd-e73e-e063-6294a90aed7eSPL ID 59d3da9b-42dd-e73e-e063-6294a90aed7eSPL set ID 59d3db05-2d63-9dbf-e063-6394a90a8dd3RxCUI 349199UNII 80M03YXJ7I

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

N453401002981 followed by a unit qualifier and the quantity

Package 53401-0029-81. 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)

Valsartan tablets are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension , to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Treatment of heart failure (NYHA class II-IV); valsartan tablets significantly reduced hospitalization for heart failure. ( 1.2 ) Post-myocardial infarction; for the reduction of cardiovascular mortality in clinically stable patients with left ventricular failure or left ventricular dysfunction following myocardial infarction. ( 1.3 ) 1.1 Hypertension Valsartan tablets are indicated for the treatment of hypertension, to lower…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204011

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

FDA NDC Directory listings under ANDA 204011
ProductStrengthForm · routeLabelerProduct NDC
ValsartanValsartan 40 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-033
ValsartanValsartan 40 mg/1TabletOralAmneal Pharmaceuticals LLC65162-837
ValsartanValsartan 80 mg/1TabletOralAmneal Pharmaceuticals LLC65162-838
ValsartanValsartan 160 mg/1TabletOralAmneal Pharmaceuticals LLC65162-839
ValsartanValsartan 320 mg/1TabletOralAmneal Pharmaceuticals LLC65162-840
ValsartanValsartan 40 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-837
ValsartanValsartan 80 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-838
ValsartanValsartan 160 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-839
ValsartanValsartan 320 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-840
ValsartanValsartan 320 mg/1TabletOralAvKARE42291-859
ValsartanValsartan 40 mg/1TabletOralAvKARE42291-856
ValsartanValsartan 80 mg/1TabletOralAvKARE42291-857
ValsartanValsartan 160 mg/1TabletOralAvKARE42291-858

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