NDC codes

FDA NDC Directory
Product NDC (as listed)68180-276Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68180-0276Add the package segment from the table below.

Product information

Brand name (proprietary)
Valsartan
Generic name (nonproprietary)
valsartan
Active ingredients
Valsartan — 40 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201677
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68180-276_b0ac78ab-2315-4aca-a405-bd86b8a08692SPL ID b0ac78ab-2315-4aca-a405-bd86b8a08692SPL set ID 9eb9d98e-7057-4ca0-91ab-2030bc0120a6RxCUI 349199, 349200, 349201, 349483UNII 80M03YXJ7IUPC 0368180279099, 0368180278092

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.

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Valsartan tablet is 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 to 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 low…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-276

What is NDC 68180-276?
68180-276 is the product NDC for Valsartan, Valsartan 40 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?
Valsartan.
What is the active ingredient?
Valsartan.
Who is the labeler?
Lupin Pharmaceuticals, Inc., NDC labeler code 68180. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Valsartan?
130 other product NDCs are listed under this name. See all Valsartan 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 Valsartan NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
valsartanValsartan 320 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-39359746-0393-3059746-0393-3259746-0393-67+1 more
ValsartanValsartan 40 mg/1Tablet, Film coatedOralLaurus Labs Limited42385-98942385-0989-0542385-0989-3042385-0989-68
ValsartanValsartan 80 mg/1Tablet, Film coatedOralLaurus Labs Limited42385-99042385-0990-0542385-0990-3042385-0990-68+1 more
ValsartanValsartan 160 mg/1Tablet, Film coatedOralLaurus Labs Limited42385-99142385-0991-0542385-0991-3042385-0991-68+1 more
ValsartanValsartan 320 mg/1Tablet, Film coatedOralLaurus Labs Limited42385-99242385-0992-0542385-0992-3042385-0992-68+1 more
ValsartanValsartan 80 mg/1Tablet, Film coatedOralCoupler LLC67046-159667046-1596-03
ValsartanValsartan 320 mg/1Tablet, Film coatedOralCoupler LLC67046-157467046-1574-03
Valsartanvalsartan oralValsartan 4 mg/mLSolutionOralAdvagen Pharma Ltd72888-18472888-0184-1372888-0184-48
ValsartanValsartan 40 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-188270771-1882-03
ValsartanValsartan 80 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-188370771-1883-09

All 131 Valsartan NDCs

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