NDC codes

FDA NDC Directory
Product NDC (as listed)62332-044Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0044Add 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
62332-044-1062332004410100 TABLET in 1 CARTON (62332-044-10)Marketed from May 20, 2016
62332-044-306233200443030 TABLET in 1 BOTTLE (62332-044-30)Marketed from May 20, 2016
62332-044-7162332004471500 TABLET in 1 BOTTLE (62332-044-71)Marketed from May 20, 2016
62332-044-906233200449090 TABLET in 1 BOTTLE (62332-044-90)Marketed from May 20, 2016
62332-044-91623320044911000 TABLET in 1 BOTTLE (62332-044-91)Marketed from May 20, 2016

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
Valsartan40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091367
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 62332-044_d9c3b1ac-bbb0-4974-b337-88e247093c72SPL ID d9c3b1ac-bbb0-4974-b337-88e247093c72SPL set ID 8478a05f-38fd-412d-af49-69a73a787c8fRxCUI 349199, 349200, 349201, 349483UNII 80M03YXJ7IUPC 0362332044306, 0362332046300

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

N462332004410 followed by a unit qualifier and the quantity

Package 62332-0044-10. 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: • Hypertension, to lower blood pressure in adults and children 6 years and older. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions (1.1) • Heart failure (NYHA class II-IV), to reduce hospitalization for heart failure in adults (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 in adults (1.3) 1.1 Hypertension Valsartan tablets are indicated for the treatment of hypertension, to lowe

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091367

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

FDA NDC Directory listings under ANDA 091367
ProductStrengthForm · routeLabelerProduct NDC
ValsartanValsartan 40 mg/1TabletOralAlembic Pharmaceuticals Limited46708-044
ValsartanValsartan 80 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-045
ValsartanValsartan 320 mg/1TabletOralAlembic Pharmaceuticals Limited46708-047
ValsartanValsartan 80 mg/1TabletOralAlembic Pharmaceuticals Limited46708-045
ValsartanValsartan 160 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-046
ValsartanValsartan 160 mg/1TabletOralAlembic Pharmaceuticals Limited46708-046
ValsartanValsartan 320 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-047

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